WO2023156529A1 - Dispositif d'étirage - Google Patents

Dispositif d'étirage Download PDF

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Publication number
WO2023156529A1
WO2023156529A1 PCT/EP2023/053903 EP2023053903W WO2023156529A1 WO 2023156529 A1 WO2023156529 A1 WO 2023156529A1 EP 2023053903 W EP2023053903 W EP 2023053903W WO 2023156529 A1 WO2023156529 A1 WO 2023156529A1
Authority
WO
WIPO (PCT)
Prior art keywords
medical device
patient
stomach wall
sensor
hydraulic
Prior art date
Application number
PCT/EP2023/053903
Other languages
English (en)
Inventor
Peter Forsell
Original Assignee
Implantica Patent Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from PCT/EP2022/073784 external-priority patent/WO2023031038A1/fr
Application filed by Implantica Patent Ltd filed Critical Implantica Patent Ltd
Publication of WO2023156529A1 publication Critical patent/WO2023156529A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F5/00—Orthopaedic methods or devices for non-surgical treatment of bones or joints; Nursing devices; Anti-rape devices
    • A61F5/0003—Apparatus for the treatment of obesity; Anti-eating devices
    • A61F5/0013—Implantable devices or invasive measures
    • A61F5/0069—Implantable devices or invasive measures in the wall of the stomach

Definitions

  • the present invention relates to medical implants. More specifically the invention relates to medical implants for stretching the stomach wall of a patient for creating a feeling of satiety.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is provided.
  • the medical device is implantable and comprises a first member configured to be fixated to a first portion of the stomach wall, and a second member configured to be fixated to a second portion of the stomach wall.
  • the medical device further comprises an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portion.
  • At least one of the first and second member is flexible in a second direction substantially perpendicular to the first direction for adapting the medical device to the curvature of the stomach of the patient and/or facilitating insertion of the medical device into the body of the patient.
  • the operation device is further configured for operating the second member to displace the second member in a third direction relative to the first member, for stretching the stomach wall between the first and second portion.
  • the medical device further comprises a third member configured to be fixated to a third portion of the stomach wall.
  • the operation device may further be configured for operating the third member to displace the third member relative to at least one of the first and second member, for stretching the stomach wall between the third portion and at least one of the first and second portions.
  • the medical device further comprises a fourth member configured to be fixated to a fourth portion of the stomach wall.
  • the operation device may further be configured for operating the fourth member to displace the fourth member relative to at least one of the first, second and third member, for stretching the stomach wall between the fourth portion and at least one of the first, second and third portions.
  • At least one of the first, second, third and fourth member is inoperably fixated to a main portion. According to one embodiment at least two of the first, second, third and fourth members are inoperably fixated the main portion. According to one embodiment at least one of the first, second, third and fourth member is operably fixated to a main portion.
  • At least two of the first, second, third and fourth members are operably fixated the main portion.
  • the main portion may comprise at least part of the operation device.
  • At least one of the first, second, third and fourth member may comprise at least part of the operation device.
  • the member being inoperably fixated to the main portion may comprise at least part of the operation device.
  • the two members being inoperably fixated to the main portion each comprises at least part of the operation device.
  • the first member is inoperably fixated to the main portion and comprises a first portion of the operation device
  • the second member is inoperably fixated to the main portion and comprises a second portion of the operation device.
  • the first portion of the operation device may be configured for operating the third member and the second portion of the operation device may be configured for operating the fourth member.
  • the first member is inoperably fixated to the main portion and comprises a first portion of the operation device, and a second portion of the operation device, wherein the first portion of the operation device is configured for operating the third member and the second portion of the operation device is configured for operating the fourth member.
  • At least one of the first, second, third and fourth member may be elongated.
  • At least one of the first, second, third and fourth member may be hinged for enabling pivotal movement.
  • At least one of the first, second, third and fourth member may be configured to be at least partially invaginated by the tissue of the stomach wall.
  • At least one of the first, second, third and fourth member comprises at least one fixation portion configured for fixation of the member to tissue of the stomach wall using at least one of sutures, staplers or tissue growth promoting structure.
  • the at least one fixation portion may comprise at least one of a through-hole and a recess for receiving the at least one of sutures or staplers.
  • the operation device in any if the embodiments may be a mechanical operation device and/or may be a hydraulic operation device.
  • the operation device comprises at least one electrical motor and the operation device may further comprises a gear system configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • the operation device is configured to be remotely powered.
  • the operation device may be remotely powered with mechanical force.
  • the medical device may further comprise a receiving portion configured to receive mechanical force, and a transmission for transforming the received mechanical force into a force for displacing at least one of the members for stretching the stomach wall.
  • the receiving portion may be configured to receive a rotating mechanical force
  • the transmission may be configured to transform the received rotating mechanical force into a liner mechanical force
  • the receiving portion is configured to receive a linear mechanical force.
  • the operation device may in some embodiments be configured to be remotely powered with hydraulic force, and the medical device may is such embodiments further comprise a receiving portion configured to receive hydraulic force, and a transmission for transforming the received hydraulic force into a force for displacing at least one of the members for stretching the stomach wall.
  • the transmission may comprise at least one hydraulic cylinder.
  • the medical device may further comprise an enclosure configured to enclose at least a portion of the operation device, and the enclosure may be flexible to enable the displacement of at least one member.
  • the enclosure may comprise the main portion.
  • the medical device may further comprise an energy storage unit for directly or indirectly energizing the medical device and a controller for controlling the operation device.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device may further comprise at least one sensor, and the controller may be configured for receiving sensor input from the at least one sensor.
  • the sensor may be a sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, and a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient and may be a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the senor is configured to sense a parameter related to the patient swallowing and may comprise at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a source external to the body of the patient.
  • the controller is configured to transmit the information based on sensor input to a source external to the body of the patient, wirelessly.
  • the medical device could in any of the embodiments herein further comprise a capacitor connected to the implantable energy storage unit and connected to the operation device, the capacitor being configured to be charged by the implantable energy storage unit and to provide the operation device with electrical power.
  • the implantable energy storage unit may be a solid-state battery.
  • the implantable energy storage unit may be a tionyl-chlorid battery.
  • the medical device may further comprise a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the controller may be configured to receive a patient generated control signal and the controller may be configured to control the operation device on the basis of the received patient generated control signal.
  • the controller may be configured to control the operation device on the basis of a signal related to a lapsed time or a time of day.
  • the controller may be configured to receive a signal from a sensor external to the body of the patient.
  • the medical device may in some embodiments further comprise an electrode arrangement configured to be arranged to engage and electrically stimulate muscle tissue of the stomach to exercise the muscle tissue to improve the conditions for long term implantation of the medical device.
  • a medical device system is further provided.
  • the medical device system comprises a medical device according to any of the embodiments herein, and an implantable remote unit connected to the medical device.
  • the implantable remote unit may comprise an energy storage unit for directly or indirectly energizing the medical device.
  • the implantable remote unit may comprise an energy receiver for wirelessly receiving energy from a source external to the body of the patient.
  • the medical device system may according to any one of the embodiments herein comprise a controller for controlling the medical device system.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the implantable remote unit may further comprise at least one sensor, and wherein the controller may be configured for receiving sensor input from the at least one sensor.
  • the sensor may be a sensor configured to sense a physical parameter of the medical device system.
  • the sensor may be a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, and a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient and may be a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the senor is configured to sense a parameter related to the patient swallowing and may comprise at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a source external to the body of the patient.
  • the controller is configured to transmit the information based on sensor input to a source external to the body of the patient, wirelessly.
  • the medical device could in any of the embodiments herein further comprise a capacitor connected to the implantable energy storage unit and connected to the operation device, the capacitor being configured to be charged by the implantable energy storage unit and to provide the operation device with electrical power.
  • the implantable energy storage unit may be a solid-state battery.
  • the implantable energy storage unit may be a tionyl-chlorid battery.
  • the medical device may further comprise a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the controller may be configured to receive a patient generated control signal and the controller may be configured to control the operation device on the basis of the received patient generated control signal.
  • the controller may be configured to control the operation device on the basis of a signal related to a lapsed time or a time of day.
  • the controller may be configured to receive a signal from a sensor external to the body of the patient.
  • the implantable remote unit comprises at least a portion of the operation device.
  • the portion of the operation device may comprise at least one electrical motor and may further comprise a gear system configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • the portion of the operation device comprises at least one hydraulic pump.
  • the medical device system may further comprise a force transferring element configured to mechanically transfer force from the implantable remote unit to the medical device.
  • the force transferring element may be configured to transfer a rotating mechanical force from the implantable remote unit to the medical device and/or a linear mechanical force from the implantable remote unit to the medical device.
  • medical device system further comprises a force transferring element configured to hydraulically transfer force from the implantable remote unit to the medical device.
  • the medical device system further comprises at least one lead for transferring electrical energy and/or information from the implantable remote unit to the medical device.
  • the medical device system further comprises at least one injection port for injecting fluid into the medical device system.
  • a method of implanting a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety comprises a first member configured to be fixated to a first portion of the stomach wall, a second member configured to be fixated to a second portion of the stomach wall and an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portions.
  • At least one of the first and second member is flexible in a second direction substantially perpendicular to the first direction.
  • the method comprises making an incision in the abdomen of the patient, for accessing the stomach, dissecting a portion of the stomach, inserting the medical device into the abdomen of the patient, using the flexibility of at least one of the first and second member for adapting the medical device to the curvature of the stomach of the patient, and fixating the first member to a first portion of the stomach wall, and fixating the second member to a second portion of the stomach wall.
  • the medical device further comprises a third member configured to be fixated to a third portion of the stomach wall, and the method further comprises the step of fixating the third member to a third portion of the stomach wall.
  • the medical device further comprises a fourth member configured to be fixated to a fourth portion of the stomach wall, and the method comprises the step of fixating the fourth member to a fourth portion of the stomach wall.
  • At least one of the first, second, third and fourth members are connected to a main portion, and the method comprises using the flexibility of at least one of the first, second, third and fourth members for adapting the medical device to the curvature of the stomach of the patient by pivoting at least one of the first, second, third and fourth members relative to the main portion.
  • at least one of the steps of fixating the first member to a first portion of the stomach wall, and fixating the second member to a second portion of the stomach wall comprises at least partially invaginated at least one of the first and second member by the tissue of the stomach wall.
  • At least one of the steps of fixating the first member to a first portion of the stomach wall, and fixating the second member to a second portion of the stomach wall comprises fixating at least one of the first and second member to tissue of the stomach wall using at least one of sutures, staplers or tissue growth promoting structure.
  • the method may further comprise placing at least one sensor in the area of the esophagus of the patient for sensing a parameter related to the patient swallowing.
  • the step of placing at least one sensor in the area of the esophagus of the patient for sensing a parameter related to the patient swallowing may comprise placing at least one of: a motility sensor, a acoustic sensor, an optical sensor or a strain sensor.
  • placing at least one sensor in the area of the stomach of the patient comprises placing a sensor for sensing a parameter related to the patient eating.
  • the step of placing at least one sensor in the area of the stomach of the patient for sensing a parameter related to the patient eating comprises placing at least one of temperature sensor, blood saturation or oxygenation sensor, a blood pressure sensor, a sensor configured to sense a parameter related to an ischemia marker, or a pH sensor.
  • the step of sensing pH may comprise sensing the acidity in the stomach.
  • the method may further comprise placing an electrode arrangement configured to be arranged between the medical device and the stomach to engage and electrically stimulate muscle tissue of the stomach to exercise the muscle tissue to improve the conditions for long term implantation of the medical device.
  • the method further comprises placing an implantable remote unit connected to the medical device in the body of the patient, and the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising at least a portion of the operation device.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising an energy storage unit.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising a wireless energy receiver.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising a wireless transceiver for wireless communication.
  • a method of implanting a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety comprising a first member configured to be fixated to a first portion of the stomach wall, a second member configured to be fixated to a second portion of the stomach wall and an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portions, wherein at least one of the first and second member is flexible in a second direction substantially perpendicular to the first direction.
  • the method comprising making an incision in the abdomen of the patient, for accessing the stomach, dissecting a portion of the stomach, using the flexibility of at least one of the first and second member for facilitating insertion of the medical implant into the body of the patient, and inserting the medical device into the abdomen of the patient.
  • the step of using the flexibility of at least one of the first and second member for facilitating insertion of the medical device into the body of the patient further comprises using the flexibility of at least one of the first and second members for compressing the medical device such that it can be inserted through an incision in the skin of the patient.
  • the step of using the flexibility of at least one of the first and second member for facilitating insertion of the medical device into the body of the patient comprises using the flexibility of at least one of the first and second members for compressing the medical device such that it can be inserted through a cannula of a trocar and into the body of the patient.
  • the step of using the flexibility of at least one of the first and second member for expanding the medical device after the medical device has been inserted into the body of the patient
  • the method further comprises the steps of fixating the first member to a first portion of the stomach wall, and fixating the second member to a second portion of the stomach wall.
  • the medical device further comprises a third member configured to be fixated to a third portion of the stomach wall, and the method further comprises the step of fixating the third member to a third portion of the stomach wall.
  • the medical device further comprises a fourth member configured to be fixated to a fourth portion of the stomach wall, and the method comprises the step of fixating the fourth member to a fourth portion of the stomach wall.
  • at least one of the first, second, third and fourth members are connected to a main portion, and the method comprises using flexibility of at least one of the first, second, third and fourth members by pivoting at least one of the first, second, third and fourth members relative to the main portion.
  • At least one of the steps of fixating the first member to a first portion of the stomach wall, and fixating the second member to a second portion of the stomach wall comprises at least partially invaginating at least one of the first and second member by the tissue of the stomach wall.
  • At least one of the steps of fixating the first member to a first portion of the stomach wall, and fixating the second member to a second portion of the stomach wall may comprise fixating at least one of the first and second member to tissue of the stomach wall using at least one of sutures, staplers or tissue growth promoting structure.
  • the method may further comprise placing at least one sensor in the area of the esophagus of the patient for sensing a parameter related to the patient swallowing.
  • the step of placing at least one sensor in the area of the esophagus of the patient for sensing a parameter related to the patient swallowing may comprise placing at least one of: a motility sensor, a acoustic sensor, an optical sensor or a strain sensor.
  • the method further comprises placing at least one sensor in the area of the stomach of the patient for sensing a parameter related to the patient eating.
  • the step of placing at least one sensor in the area of the stomach of the patient for sensing a parameter related to the patient eating may comprise placing at least one of temperature sensor, blood saturation or oxygenation sensor, a blood pressure sensor, a sensor configured to sense a parameter related to an ischemia marker, or a pH sensor.
  • the step of sensing pH comprises sensing the acidity in the stomach.
  • the method further comprises placing an electrode arrangement configured to be arranged between the medical device and the stomach to engage and electrically stimulate muscle tissue of the stomach to exercise the muscle tissue to improve the conditions for long term implantation of the medical device.
  • the method further comprises placing an implantable remote unit connected to the medical device in the body of the patient.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising at least a portion of the operation device.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising an energy storage unit.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising a wireless energy receiver.
  • the step of placing an implantable remote unit connected to the medical device in the body of the patient may comprise placing an implantable remote unit comprising a wireless communication unit.
  • a method of calibrating a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the medical device comprising a first member configured to be fixated to a first portion of the stomach wall, a second member configured to be fixated to a second portion of the stomach wall and an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portions, and a controller comprising a transceiver for wireless communication.
  • the method comprising: receiving, at the controller, a first input signal comprising at least one of a sensor input signal related to a physical parameter of the medical device, and an input signal from a source external to the body of the patient.
  • the method further comprises controlling, by the controller, the operation device to adjust the stretching of the stomach wall, in response to the first input signal, and receiving, at the transceiver, a second input signal from the source external to the patient, and controlling, by the controller, the operation device to further adjust the stretching of the stomach wall, in response to the second input signal.
  • the sensor input signal related to a physical parameter of the medical device is a sensor input related to at least one of: energy consumption, position of at least one of the first member, the second member and the operation device, strain on at least one of the first member, the second member and the operation device, and speed of the operation device.
  • the input signal from a source external to the body of the patient is an input signal generated by the patient.
  • the input signal generated by the patient is an input signal related to at least one of: a feeling of satiety experienced by the patient, a feeling of pain experienced by the patient, and the patient ingesting something.
  • the step of adjusting the stretching of the stomach wall comprises adjusting one of: the force with which the stomach wall is stretched, the speed with which the stomach wall is stretched, and the duration of the stretching of the stomach wall.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the medical device being implantable and comprising: a first member comprising a first stomach engager configured to be fixated to a first portion of the stomach wall, a second member comprising a second stomach engager portion configured to be fixated to a second portion of the stomach wall, an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portions, and a main portion.
  • the first and second members are connected to the main portion, and at least the second member is pivotally connected to the main portion, such that the second member can be displaced in the first direction relative to the first member by the second member pivoting in relation to the main portion.
  • the operation device comprises at least one eccentric rotatable engagement member configured to engage at least the second member such that the eccentric rotation of the engagement member causes the second member to pivot in relation to the main portion for displacing the second member relative to the first member for stretching the stomach wall between the first and second portions.
  • the at least one eccentric rotatable engagement member is configured to engage the second member at a distance from the point of pivot of the second member.
  • the eccentric rotatable engagement member comprises at least one of a recess or protrusion
  • the second member comprises at least one of a recess or protrusion. The engagement between the recess or protrusion of the engagement member and the recess or protrusion of the second member causes the second member to pivot in relation to the main portion for displacing the second member in the first direction relative to the first member.
  • the first member is pivotally connected to the main portion, such that the first member can be displaced relative to at least one of the second member and a third member, by the first member pivoting in relation to the main portion.
  • the operation device is configured to simultaneously displace the second member in the first direction and the first member in a second direction to thereby increase the distance between the first stomach engager portion and the second stomach engager portion to stretch the stomach wall between the first portion of the stomach wall and the second portion of the stomach wall.
  • the operation device comprises a radial engagement surface configured to radially engage at least the second member such that the eccentric rotation of the engagement member causes the second member to pivot in relation to the main portion.
  • At least the second member is configured to be operated in the first direction by the eccentric rotation of the engagement member and in an opposite direction by an elastic element.
  • the eccentric rotatable engagement member comprises a groove encircling the center of rotation of the eccentric rotatable engagement member.
  • the groove may be configured to control the movement of at least the second member in the first direction and in the opposite direction.
  • the groove may be configured to control the movement of at least the second member at all times.
  • the medical device comprises the first member, the second member, the third member and a fourth member, and wherein: the first, second, third and fourth members are all pivotally connected to the main portion, the groove is configured to control the movement of the first, second, third and fourth members in a first direction and in an opposite direction, and as the eccentric rotatable engagement member comprising the groove rotates, the first, second, third and fourth members are sequentially displaced in relation to the main portion in the first direction and in the opposite direction for sequentially stretching the stomach wall portions between the members.
  • the eccentric rotatable engagement member comprising the groove rotates: the first and second members are simultaneously displaced, or the second and third members are simultaneously displaced, or the third and fourth members are simultaneously displaced.
  • At least one of the first, second, third and fourth member is configured to be at least partially invaginated by the tissue of the stomach wall.
  • At least one of the first, second, third and fourth member comprises at least one fixation portion configured for fixation of the member to tissue of the stomach wall using at least one of sutures, staplers or tissue growth promoting structure.
  • the at least one fixation portion may comprise at least one of a through-hole and a recess for receiving the at least one of sutures or staplers.
  • the operation device in any of the embodiments herein may comprise at least one electrical motor which may be connected to a gear system configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • the operation device is configured to be remotely powered.
  • the operation device may be configured to be remotely powered with mechanical force.
  • the medical device may further comprise an enclosure configured to enclose at least a portion of the operation device, and the enclosure may be flexible to enable the displacement of at least one member.
  • the enclosure may comprise the main portion.
  • the medical device may further comprise an energy storage unit for directly or indirectly energizing the medical device and a controller for controlling the operation device.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device may further comprise at least one sensor, and the controller may be configured for receiving sensor input from the at least one sensor.
  • the sensor may be a sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, and a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient and may be a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the senor is configured to sense a parameter related to the patient swallowing and may comprise at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a source external to the body of the patient.
  • the controller is configured to transmit the information based on sensor input to a source external to the body of the patient, wirelessly.
  • the medical device could in any of the embodiments herein further comprise a capacitor connected to the implantable energy storage unit and connected to the operation device, the capacitor being configured to be charged by the implantable energy storage unit and to provide the operation device with electrical power.
  • the implantable energy storage unit may be a solid-state battery.
  • the implantable energy storage unit may be a tionyl-chlorid battery.
  • the medical device may further comprise a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the controller may be configured to receive a patient generated control signal and the controller may be configured to control the operation device on the basis of the received patient generated control signal.
  • the controller may be configured to control the operation device on the basis of a signal related to a lapsed time or a time of day.
  • the controller may be configured to receive a signal from a sensor external to the body of the patient.
  • the medical device may in some embodiments further comprise an electrode arrangement configured to be arranged to engage and electrically stimulate muscle tissue of the stomach to exercise the muscle tissue to improve the conditions for long term implantation of the medical device.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the medical device being implantable and comprising first member comprising a first stomach engager configured to be fixated to a first portion of the stomach wall and a second member comprising a second stomach engager portion configured to be fixated to a second portion of the stomach wall.
  • the medical device further comprises a hydraulic operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portions, and a main portion.
  • the first and second members are connected to the main portion, and at least the second member is configured to bend or pivot in relation to the main portion, such that the second member can be displaced in the first direction relative to the first member by the second member bending or pivoting in relation to the main portion.
  • At least the second member comprises a fluid chamber at least partially enclosed by a flexible wall portion, and the flexible wall portion causes the second member to bend or pivot when hydraulic fluid is moved to or from the fluid chamber for stretching the stomach wall between the first and second portions.
  • the flexible wall portion comprises elevated and lowered portions.
  • the elevated and lowered portions may be configured to enable the second member to bend or pivot when fibrotic tissue is covering the elevated and lowered portions.
  • the flexible wall portion comprises at least one pleated portion such as a bellows.
  • the second member comprises a pivoting element pivotally fixated to the main portion, the flexible wall portion causes the pivoting element to pivot when hydraulic fluid is moved to or from the fluid chamber for stretching the stomach wall between the first and second portions.
  • the second member comprises a second fluid chamber partially enclosed by a flexible wall portion, and wherein the bending or pivoting of the second member is caused by the altering the relationship between the fluid levels in the first and second fluid chamber.
  • the bending or pivoting of the second member is caused by at least one of: movement of fluid from the first fluid chamber, and movement of fluid to the second fluid chamber.
  • the second member is configured to be displaced: in the first direction relative to the first member by the movement of fluid from the first fluid chamber, and in a second direction relative to the first member by the movement of fluid from the second fluid chamber.
  • the second member is configured to be displaced: in the first direction relative to the first member by the movement of fluid to the first fluid chamber, and in a second direction relative to the first member by the movement of fluid to the second fluid chamber.
  • the first member may comprise a fluid chamber at least partially enclosed by a flexible wall portion, and wherein the flexible wall portion may cause the first member to bend or pivot when hydraulic fluid is moved to or from the fluid chamber.
  • the medical device comprises at least one of a third member comprising a fluid chamber at least partially enclosed by a flexible wall portion, and wherein the flexible wall portion causes the third member to bend or pivot when hydraulic fluid is moved to or from the fluid chamber, a fourth member comprising a fluid chamber at least partially enclosed by a flexible wall portion, and wherein the flexible wall portion causes the fourth member to bend or pivot when hydraulic fluid is moved to or from the fluid chamber, and a fifth member comprising a fluid chamber at least partially enclosed by a flexible wall portion, and wherein the flexible wall portion causes the fifth member to bend or pivot when hydraulic fluid is moved to or from the fluid chamber.
  • the medical device further comprises at least one operable valve configured to operate to at least one of: switch between distributing hydraulic fluid to or from the fluid chamber of the first member and to or from the fluid chamber of the second member, switch between distributing hydraulic fluid to or from the fluid chamber of the first member and to or from the fluid chamber of the second member and to or from the fluid chamber of the third member, switch between distributing hydraulic fluid to or from the fluid chamber of the first member and to or from the fluid chamber of the second member and to or from the fluid chamber of the third member and to or from the fluid chamber of the fourth member, and switch between distributing hydraulic fluid to or from the fluid chamber of the first member and to or from the fluid chamber of the second member and to or from the fluid chamber of the third member and to or from the fluid chamber of the fourth member and to or from the fluid chamber of the fifth member.
  • the at least one operable valve is a rotatable operable valve.
  • the medical device further comprises an actuator for operating the operable valve, and the actuator is at least one of: an electric actuator and a hydraulic actuator.
  • the operable valve is configured to simultaneously distribute fluid to the first fluid chamber of the first member and the second fluid chamber of the second member, for causing the first and second members to bend or pivot in different directions, away from each other, for stretching the stomach wall between the first and second member.
  • the operable valve is configured to simultaneously distribute fluid to the first fluid chamber of the second member and the second fluid chamber of the third member, for causing the second and third members to bend or pivot in different directions, away from each other, for stretching the stomach wall between the second and third member.
  • each of the first, second, third, fourth and fifth member comprises a stomach engager portion.
  • the stomach engager portion may be configured to be invaginated by the stomach wall using stomach-to-stomach sutures or staplers.
  • the stomach engager portion may comprise at least one of a fixation portion configured for fixation of the stomach engager portion to tissue of the stomach wall using at least one of sutures and staplers, and a tissue growth promoting structure such that the stomach engager portion can be fixated to the stomach wall by in-growth of fibrotic tissue.
  • the main portion comprises a fluid conduit for conducting fluid to at least one of the first, second, third, fourth and fifth member.
  • the medical device further comprises an implantable hydraulic pump for pumping fluid to the fluid conduit.
  • the implantable pump may be configured to be positioned at a remote location in relation to the main portion.
  • the medical device may further comprises an energy storage unit for directly or indirectly energizing the medical device and a controller for controlling at least one of the pump and the operable valve.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device may further comprise at least one sensor, and the controller may be configured for receiving sensor input from the at least one sensor.
  • the sensor may be a sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, and a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient and may be a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the senor is configured to sense a parameter related to the patient swallowing and may comprise at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a source external to the body of the patient.
  • the controller is configured to transmit the information based on sensor input to a source external to the body of the patient, wirelessly.
  • the medical device could in any of the embodiments herein further comprise a capacitor connected to the implantable energy storage unit and connected to the operation device, the capacitor being configured to be charged by the implantable energy storage unit and to provide the operation device with electrical power.
  • the implantable energy storage unit may be a solid-state battery.
  • the implantable energy storage unit may be a tionyl-chlorid battery.
  • the medical device may further comprise a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the controller may be configured to receive a patient generated control signal and the controller may be configured to control the operation device on the basis of the received patient generated control signal.
  • the controller may be configured to control the operation device on the basis of a signal related to a lapsed time or a time of day.
  • the controller may be configured to receive a signal from a sensor external to the body of the patient.
  • the medical device may in some embodiments further comprise an electrode arrangement configured to be arranged to engage and electrically stimulate muscle tissue of the stomach to exercise the muscle tissue to improve the conditions for long term implantation of the medical device.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the medical device being implantable and comprising: a first member comprising a first stomach engager configured to be fixated to a first portion of the stomach wall and a second member comprising a second stomach engager portion configured to be fixated to a second portion of the stomach wall.
  • the medical device further comprises an operation device for operating the second member to displace the second member in a first direction, for stretching the stomach wall between the first and second portions, and a main portion.
  • the first and second members are connected to the main portion, and at least the second member is configured to bend or pivot in relation to the main portion, such that the second member can be displaced in a direction away from the first member by the second member bending or pivoting in relation to the main portion.
  • the operation device comprises a first flexible cable for pulling on the second member for displacing the second member in the direction away from the first member, and the first flexible cable is fixated to the second member at the distal half of thereof.
  • the second member comprises a flexible wall portion, and wherein the first flexible cable is at least partially enclosed by the flexible wall portion.
  • the flexible wall portion may comprise elevated and lowered portions and the elevated and lowered portions may be configured to enable the second member to bend or pivot when fibrotic tissue is covering the elevated and lowered portions.
  • the flexible wall portion comprises at least one pleated portion, such as a bellows.
  • the second member comprises a pivoting element pivotally fixated to the main portion, and wherein the first flexible cable causes the pivoting element to pivot when operated for stretching the stomach wall between the first and second portions.
  • the operation device comprises a second flexible cable for pulling on the second member for displacing the second member in a direction towards the first member, and the second flexible cable is fixated to the second member at the distal half thereof.
  • the first member is configured to bend or pivot in relation to the main portion, such that the first member can be displaced in a direction away from the second member by the first member bending or pivoting in relation to the main portion.
  • the first flexible cable is further fixated to the first member, such that pulling on the first flexible cable causes the second member to displace in the direction away from the first member, and the first member to displace in the direction away from the second member, for stretching the stomach wall between the first and second portions.
  • the medical device comprises at least one of a third member configured to bend or pivot in relation to the main portion, a fourth member configured to bend or pivot in relation to the main portion, and a fifth member configured to bend or pivot in relation to the main portion.
  • a second cable is connected to the second and third members, at the distal half thereof, such that pulling on the cable causes the second member to displace in a direction away from the third member, and the third member to displace in a direction away from the second member.
  • a third cable is connected to the third and fourth members, at the distal half thereof, such that pulling on the cable causes the third member to displace in a direction away from the fourth member, and the fourth member to displace in a direction away from the third member.
  • a fourth cable is connected to the fourth and fifth members, at the distal half thereof, such that pulling on the cable causes the fourth member to displace in a direction away from the fifth member, and the fifth member to displace in a direction away from the fourth member.
  • a fifth cable is connected to the fifth and first members, at the distal half thereof, such that pulling on the cable causes the fifth member to displace in a direction away from the first member, and the first member to displace in a direction away from the fifth member.
  • the medical device further comprises an operation device configured to pull on at least one of: the first cable, the second cable, the third cable, the fourth cable, and the fifth cable.
  • the operation device is configured to at least one of: switch between pulling on the first cable and the second cable, switch between pulling on the second cable and the third cable, switch between pulling on the third cable and the fourth cable, and switch between pulling on the fourth cable and the fifth cable.
  • the operation device may be a rotatable operation device.
  • the operation device may comprise at least one eccentric rotatable engagement member configured to engage at least the first flexible cable for pulling the first flexible wire.
  • the eccentric rotatable engagement member may further be configured to engage at least one of: the second flexible cable, the third flexible cable, the fourth flexible cable, and the fifth flexible cable.
  • the eccentric rotatable engagement member comprises at least one of a recess or protrusion
  • at least the first flexible cable is fixated to at least one of a recess or protrusion
  • the engagement between the recess or protrusion of the engagement member and the recess or protrusion of the second member causes the second member to pivot in relation to the main portion for displacing the second member in the first direction relative to the first member.
  • at least the second member is configured to be operated in the first direction by the first flexible cable and in an opposite direction by an elastic element.
  • the eccentric rotatable engagement member comprises a groove encircling the center of rotation of the eccentric rotatable engagement member.
  • the groove is configured to control the movement of at least the second member in the first direction and in the opposite direction.
  • stomach engager portions may in any of the embodiments herein be configured to be invaginated by the stomach wall using stomach-to-stomach sutures or staplers.
  • the stomach engager portions may comprise at least one of: a fixation portion configured for fixation of the stomach engager portion to tissue of the stomach wall using at least one of sutures and staplers, and a tissue growth promoting structure such that the stomach engager portion can be fixated to the stomach wall by in-growth of fibrotic tissue.
  • the operation device may in any of the embodiments herein comprises at least one electrical motor which may be connected to a gear system configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • the operation device may partially be positioned at a remote location in the body of the patient, in relation to the main portion.
  • the medical device may further comprises an energy storage unit for directly or indirectly energizing the medical device and a controller for controlling at least one of the pump and the operable valve.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device may further comprise at least one sensor, and the controller may be configured for receiving sensor input from the at least one sensor.
  • the sensor may be a sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, and a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient and may be a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the senor is configured to sense a parameter related to the patient swallowing and may comprise at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a source external to the body of the patient.
  • the controller is configured to transmit the information based on sensor input to a source external to the body of the patient, wirelessly.
  • the medical device could in any of the embodiments herein further comprise a capacitor connected to the implantable energy storage unit and connected to the operation device, the capacitor being configured to be charged by the implantable energy storage unit and to provide the operation device with electrical power.
  • the implantable energy storage unit may be a solid-state battery.
  • the implantable energy storage unit may be a tionyl-chlorid battery.
  • the medical device may further comprise a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the controller may be configured to receive a patient generated control signal and the controller may be configured to control the operation device on the basis of the received patient generated control signal.
  • the controller may be configured to control the operation device on the basis of a signal related to a lapsed time or a time of day.
  • the controller may be configured to receive a signal from a sensor external to the body of the patient.
  • the medical device may in some embodiments further comprise an electrode arrangement configured to be arranged to engage and electrically stimulate muscle tissue of the stomach to exercise the muscle tissue to improve the conditions for long term implantation of the medical device.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the medical device being implantable and comprising a first member comprising a first stomach engager configured to engage a first portion of the stomach wall, a second member comprising a second stomach engager portion configured to engage a second portion of the stomach wall, and a main portion.
  • the first and second members are connected to the main portion.
  • the medical device further comprises an operation device for operating at least the second member to displace the second member in a direction away from the first member, for stretching the stomach wall between the first and second portions, wherein a portion of the operation device is placed in a remote unit configured to be placed at a remote location in the body of the patient, and a force transferring element configured to transfer force hydraulically or mechanically from the remote unit to the main portion, for operating the second member.
  • the second member is configured to bend or pivot in relation to the main portion, such that the second member can be displaced in a direction away from the first member.
  • the first member is configured to bend or pivot in relation to the main portion, such that the first member can be displaced in a direction away from the second member.
  • the medical device further comprises a third member configured to engage a third portion of the stomach wall.
  • the medical device further comprises a fourth member configured to engage a fourth portion of the stomach wall.
  • the operation device is further configured for operating at least one of the first, third and fourth member to displace one of the first, third and fourth member relative to the main portion for stretching the stomach wall.
  • the main portion comprises at least part of the operation device.
  • At least one of the first, second, third and fourth member comprises at least part of the operation device.
  • At least one of the first, second, third and fourth member is elongated.
  • At least one of the first, second, third and fourth member is hinged for enabling pivotal movement.
  • At least one of the first, second, third and fourth member is configured to be at least partially invaginated by the tissue of the stomach wall.
  • the main portion is configured to be at least partially invaginated by the tissue of the stomach wall.
  • At least one of the first, second, third and fourth member comprises at least one fixation portion configured for fixation of the member to tissue of the stomach wall using at least one of sutures, staplers or tissue growth promoting structure.
  • the portion of the operation device placed in the remote unit comprises at least one electrical motor.
  • the portion of the operation device placed in the remote unit further comprises a gear system configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • a portion of the operation device is placed in the main portion, and the portion of the operation device placed in the main portion comprises a receiving portion configured to receive mechanical force, and a transmission for transforming the received mechanical force into a force for displacing at least one of the members for stretching the stomach wall.
  • the transmission may comprise a gear system configured to reduce the speed and increase the force of the received mechanical force.
  • the receiving portion is configured to receive a rotating mechanical force
  • the transmission is configured to transform the received rotating mechanical force into a liner mechanical force
  • the receiving portion is configured to receive a linear mechanical force.
  • a portion of the operation device is placed in the main portion.
  • the portion of the operation device placed in the main portion comprises a receiving portion configured to receive hydraulic force, and a transmission for transforming the received hydraulic force into a force for displacing at least one of the members for stretching the stomach wall.
  • the transmission comprises at least one hydraulic cylinder.
  • the portion of the operation device placed in the main portion comprises at least one operable valve.
  • the portion of the operation device placed in the remote unit may comprise at least one operable valve.
  • the operable valve is configured to control the flow of hydraulic fluid from a first state in which the hydraulic fluid can operate the first member to a second state in which the hydraulic fluid can operate the second member.
  • the portion of the operation device placed in the remote unit may comprise at least one hydraulic pump.
  • the remote unit may comprise a hydraulic reservoir for holding a hydraulic fluid.
  • the remote unit may comprise an injection port for at least one of injecting and removing hydraulic fluid from the medical device.
  • the remote unit further comprises an energy storage unit for directly or indirectly energizing the medical device.
  • the remote unit further comprises a controller for controlling the operation device.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device comprises at least one sensor
  • the controller may be configured for receiving sensor input from the at least one sensor.
  • the senor is a sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient and may be a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the senor is configured to sense a parameter related to the patient swallowing and may comprise at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a source external to the body of the patient.
  • the controller is configured to transmit the information based on sensor input to a source external to the body of the patient, wirelessly.
  • the remote unit could in any of the embodiments herein further comprise a capacitor connected to the implantable energy storage unit and connected to the operation device, the capacitor being configured to be charged by the implantable energy storage unit and to provide the operation device with electrical power.
  • the remote unit may further comprise a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the controller may be configured to receive a patient generated control signal and the controller may be configured to control the operation device on the basis of the received patient generated control signal.
  • the controller may be configured to control the operation device on the basis of a signal related to a lapsed time or a time of day.
  • the medical device could further comprises at least one lead for transferring electrical energy and/or information from the remote unit to the main portion.
  • the medical device further comprises a housing configured to enclose the remote unit.
  • a first portion of the housing may be made from titanium and a second portion of the housing may be made from a ceramic material.
  • the portion of the housing made from a ceramic material comprises at least one coil embedded in the ceramic material.
  • the portion of the housing made from a ceramic material comprises at least one lead embedded in the ceramic material, for transferring electrical energy and/or information through the enclosure.
  • the remote unit comprises a magnetic coupling for transferring mechanical through the housing.
  • the remote unit may in any of the embodiments herein comprise a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprises a first surface configured to engage a first tissue surface of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second portion having a second cross-sectional area in a second plane and comprises a second surface configured to engage a second tissue surface of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion, the connecting portion having a third cross-sectional area in a third plane and is configured to connect the first portion to the second portion.
  • the first, second and third planes are parallel to each other and the third cross-sectional area is smaller than the first and second cross-sectional areas, such that the first and second portions are prevented from travelling through the hole in the tissue portion in a direction perpendicular to the first, second and third planes.
  • the first portion comprises a first wireless energy receiver for receiving energy transmitted wirelessly from an external wireless energy transmitter, and an internal wireless energy transmitter configured to transmit energy wirelessly to the second portion, and the second portion comprises a second wireless energy receiver for receiving energy from the first portion wirelessly.
  • the remote unit comprises a first energy storage unit connected to the first wireless energy receiver, and the second portion comprises a second energy storage unit connected to the second wireless energy receiver.
  • the first wireless energy receiver is configured to receive energy from the external wireless energy transmitter and store the received energy in the first energy storage unit
  • the wireless energy transmitter is configured to transmit energy stored in the first energy storage unit to the second wireless energy receiver
  • the second wireless energy receiver is configured to receive energy from the internal wireless energy transmitter and store the received energy in the second energy storage unit.
  • the first portion comprises a first wireless communication receiver for receiving wireless communication from an external device, and the first portion comprises a first wireless communication transmitter for transmitting wireless communication to a second wireless communication receiver in the second portion.
  • the first portion is detachably connected to at least one of the second portion and the connecting portion.
  • the connecting portion comprising a flange having a flange area being larger than the third cross-sectional area, such that the flange is hindered from travelling through the hole in the tissue portion, such that the second portion and the connecting portion can be held in position by the tissue portion of the patient also when the first portion is disconnected from the connecting portion.
  • the connecting portion may in any of the embodiments herein comprise a conduit for transferring a fluid from the first portion to the second portion.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the medical device being implantable and comprising a first member comprising a closed curve, the first member comprising a first portion comprising a first stomach engager configured to engage a first portion of the stomach wall and a second portion comprising a second stomach engager configured to engage a second portion of the stomach wall, wherein the first member is operable such that the first and second portion can move towards each other or away from each other for stretching a portion of the stomach wall.
  • the first member is configured to encircle a portion of the stomach wall of the patient.
  • the first member comprises a simple closed curve.
  • the first member is ring shaped.
  • the first member is operable to assume an oval shape.
  • the first member is operable to assume an elliptical shape.
  • the first and second portions moving away from each other causes a stretching of a portion of the stomach wall between the first and second portions.
  • the first member further comprises a third portion comprising a third stomach engager configured to engage a third portion of the stomach wall and a fourth portion comprising a fourth stomach engager configured to engage a fourth portion of the stomach wall, and wherein the first and second portions moving towards each other causes the third and fourth portions to move away from each other.
  • the third and fourth portions moving away from each other causes a stretching of a portion of the stomach wall between the third and fourth portions.
  • the first member is configured to be operated to stretch the stomach wall between the first member and a second member fixated to the stomach wall.
  • the first and second portions moving towards each causes a stretching of the stomach wall between at least one of the first and second portion, and the second member.
  • the medical device further comprises a second member configured to act as a support against the force created by the operation of the first member, such that the stomach wall between the first and second member can be stretched.
  • the support is configured to be fixated to the stomach wall of the patient.
  • the support may comprise a closed curve.
  • the first member is mechanically operable and may in such cases comprise a mechanical operation device.
  • the mechanical operation device may comprise at least one flexible element, directly or indirectly fixated to the first and second portion of the first member.
  • the flexible element is configured to operate the first member for at least one of: moving the first portion towards the second portion, and moving the first portion away from the second portion.
  • the mechanical operation device may comprise at least one second flexible element, directly or indirectly fixated to the third and fourth portion of the first member.
  • the flexible element may be configured to operate the first member for at least one of: moving the third portion towards the fourth portion, and moving the third portion away from the fourth portion.
  • the mechanical operation device comprises at least one third flexible element, directly or indirectly fixated to a fifth and sixth portion of the first member.
  • the flexible element may be configured to operate the first member for at least one of: moving the fifth portion towards the sixth portion, and moving the fifth portion away from the sixth portion.
  • the mechanical operation device comprises at least one fourth flexible element, directly or indirectly fixated to a seventh and eight portion of the first member.
  • the flexible element may be configured to operate the first member for at least one of: moving the seventh portion towards the eight portion, and moving the seventh portion away from the eight portion.
  • at least one of the first and second members comprises at least one recess or channel, and wherein at least one of the flexible elements travels at least partially in the recess or channel.
  • a first portion of the flexible element is directly or indirectly fixated to the first portion of the first member, and a second portion of the flexible element is directly or indirectly fixated to the second portion of the first member, such that operation of the flexible element simultaneously operates the first and second portion of the first member.
  • the medical device may further comprise at least one sheath, and the least one flexible element may be configured to travel through the sheath.
  • the sheath comprises elevated and lowered portions, such that the sheath can remain flexible even as fibrotic tissue overgrows the sheath.
  • the first member is hydraulically operable and in such cases the medical device may further comprise a hydraulic operation device.
  • the hydraulic operation device may comprise at least one hydraulic actuator, directly or indirectly fixated to the first and second portion of the first member.
  • the hydraulic actuator may be configured to operate the first member for at least one of: moving the first portion towards the second portion, and moving the first portion away from the second portion.
  • the hydraulic operation device comprises at least one second hydraulic actuator, directly or indirectly fixated to the third and fourth portion of the first member, and wherein the hydraulic actuator is configured to operate the first member for at least one of: moving the third portion towards the fourth portion, and moving the third portion away from the fourth portion.
  • the hydraulic operation device comprises at least one third hydraulic actuator, directly or indirectly fixated to a fifth and sixth portion of the first member, and wherein the hydraulic actuator is configured to operate the first member for at least one of: moving the fifth portion towards the sixth portion, and moving the fifth portion away from the sixth portion.
  • the hydraulic operation device comprises at least one fourth hydraulic actuator, directly or indirectly fixated to a seventh and eight portion of the first member.
  • the hydraulic actuator being configured to operate the first member for at least one of: moving the seventh portion towards the eight portion, and moving the seventh portion away from the eight portion.
  • the medical device comprises at least one hydraulic conduit for conducting a hydraulic fluid to at least one of the hydraulic actuators.
  • At least one of the first and second members comprises at least one recess or channel
  • the hydraulic conduit may be configured to travel at least partially in the recess or channel
  • At least one of the first and second members comprises at least one channel for conducting a hydraulic fluid.
  • the medical device may in one embodiment further comprise at least one sheath.
  • the at least one hydraulic actuator may be configured to travel through the sheath.
  • the sheath comprises elevated and lowered portions, such that the sheath can remain flexible even as fibrotic tissue overgrows the sheath.
  • the first member is flexible and/or elastic.
  • the first member is more flexible than the second member.
  • the first member is more elastic than the second member.
  • the second member is substantially rigid.
  • a major portion of the second member may be made from a material having a modulus of elasticity in the range 0,2 GPa - 1000 GPa or in the range 1 GPa - 400 GPa.
  • the second member may have a modulus of elasticity in the range 0,2 GPa - 1000 GPa or in the range 1 GPa - 400 GPa.
  • At least one of the first and second member may be configured to be invaginated by the stomach wall using stomach-to-stomach sutures or staplers.
  • At least one of the stomach engagers comprises at least one of: a fixation portion configured for fixation of the stomach engager to tissue of the stomach wall using at least one of sutures and staplers, and a tissue growth promoting structure such that the stomach engager can be fixated to the stomach wall by in-growth of fibrotic tissue.
  • a portion of the mechanical or hydraulic operation device may be placed in a remote unit configured to be placed at a remote location in the body of the patient.
  • the medical device may further comprise a force transferring element configured to transfer force hydraulically or mechanically from the remote unit to the first member, for operating the first member.
  • the portion of the operation device placed in the remote unit may comprise at least one electrical motor.
  • the portion of the operation device placed in the remote unit may further comprise a gear system configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • the portion of the operation device placed in the remote unit comprises at least one pulley for propelling the flexible element.
  • the portion of the operation device placed in the remote unit may comprise at least one hydraulic pump.
  • the remote unit may comprise a hydraulic reservoir for holding a hydraulic fluid.
  • the remote unit comprises an injection port for at least one of injecting and removing hydraulic fluid from the medical device.
  • the remote unit may further comprise an energy storage unit for directly or indirectly energizing the medical device.
  • the remote unit may further comprise a controller for controlling the operation device.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device further comprising at least one sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in at least one of the first and second members, a parameter related to a status of the energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, a hydraulic pressure in at least one of the hydraulic actuator, the hydraulic pump, the hydraulic reservoir and the hydraulic conduit.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is provided.
  • the medical device being implantable and comprising a first member configured to be fixated to a first portion of the stomach wall, a second member configured to be fixated to a second portion of the stomach wall, and an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portion.
  • the medical device further comprises an acoustic sensor configured to sense at least one sound related to the patient swallowing, and a controller configured to receive a signal from the acoustic sensor, and control the operation device on the basis of the signal received from the acoustic sensor.
  • the acoustic sensor comprises at least one microphone.
  • the acoustic sensor comprises an implantable acoustic sensor.
  • the controller is configured to receive an acoustic sensor signal from an acoustic sensor being placed external to the body of the patient.
  • the sensor may further be configured to sense at least one parameter related to a functional status of the medical device, which may be a at least one parameter related to the operation of the operation device.
  • the operation device comprises an electrical motor
  • the sensor may be configured to sense at least one parameter related to the operation of the electrical motor.
  • a method of detecting that a patient swallows is further provided. The method comprises receiving a wireless signal from an implanted acoustic sensor configured to sense at least one sound related to the patient swallowing.
  • a method of implanting s medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is further provided.
  • the method comprising fixating the medical device to the stomach wall of the patient, and implanting at least one acoustic sensor configured to sense at least one sound related to the patient swallowing.
  • the controller may comprise at least one unit having a sleep mode and an active mode, and the unit consumes less energy in the sleep mode than in the active mode.
  • the unit is configured to switch from the sleep mode to the active mode on the basis of at least one signal from the acoustic sensor.
  • the unit could for example be a DSP (Digital Signal Processor), another type of processor or a wake-up circuit of the controller, which in turn activates the functions of the controller.
  • the unit may be configured to switch from the sleep mode to the active mode on the basis of a signal from the acoustic sensor related to the patient swallowing a number of times and/or on the basis of a signal from the acoustic sensor related to the patient swallowing a number of times during a time period.
  • the controller could further comprise at least one filtering unit configured to filter acoustic signals related to at least one of: speech, the swallowing of saliva and chewing.
  • the filter could be a digital filter implemented as hardware or software in the controller and could have the filter characteristics of a high, low or bandpass filter.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is provided.
  • the medical device being implantable and comprising a first member configured to be fixated to a first portion of the stomach wall, a second member configured to be fixated to a second portion of the stomach wall, and an operation device for operating the second member to displace the second member in a first direction relative to the first member, for stretching the stomach wall between the first and second portion.
  • the medical device further comprises a sensor configured to sense at least one parameter related to the patient swallowing, and be fixated to a structure of the body comprising bone.
  • the medical device further comprises a controller configured to receive a signal from the sensor, and control the operation device on the basis of the signal received from the sensor.
  • the senor comprises at least one acoustic sensor, which may be an acoustic sensor comprising at least one microphone.
  • the senor comprises at least one accelerometer.
  • the sensor comprises at least one piezo-electric or piezo- resistive sensor.
  • the senor comprises a strain gauge.
  • the senor is configured to be fixated to at least one of: a sternum, and at least one rib of the patient.
  • the sensor configured to be fixated to the sternum or the at least one rib of the patient may be configured to be fixated to the sternum or the at least one rib of the patient, on the anterior side thereof.
  • the sensor configured to be fixated to the sternum or the at least one rib of the patient may be configured to be fixated to the sternum or the at least one rib of the patient, on the posterior side thereof.
  • the sensor may comprise an implantable sensor.
  • the senor is configured to be fixated to the structure of the body comprising bone, on the outside of the skin of the patient.
  • the controller is configured to receive a sensor signal from a sensor being placed external to the body of the patient.
  • the sensor may be configured to sense at least one parameter related to a functional status of the medical device.
  • the senor is configured to sense at least one parameter related to the operation of the operation device.
  • the controller may comprise at least one unit having a sleep mode and an active mode, and the unit consumes less energy in the sleep mode than in the active mode.
  • the unit is configured to switch from the sleep mode to the active mode on the basis of at least one signal from the sensor.
  • the unit could for example be a DSP (Digital Signal Processor), another type of processor or a wake-up circuit of the controller, which in turn activates the functions of the controller.
  • the unit may be configured to switch from the sleep mode to the active mode on the basis of a signal from the sensor related to the patient swallowing a number of times and/or on the basis of a signal from the sensor related to the patient swallowing a number of times during a time period.
  • the controller could further comprise at least one filtering unit configured to filter acoustic signals related to at least one of: speech, the swallowing of saliva and chewing.
  • the filter could be a digital filter implemented as hardware or software in the controller and could have the filter characteristics of a high, low or bandpass filter.
  • a method of detecting that a patient swallows comprises receiving a wireless signal from an implanted sensor fixated to a structure of the body comprising bone and being configured to sense at least one sound related to the patient swallowing.
  • a method of implanting s medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety comprises fixating the medical device to the stomach wall of the patient, and fixating at least one sensor configured to sense at least one parameter related to the patient swallowing to a structure of the body comprising bone.
  • a medical device for actively stretching a stomach wall of a patient for creating a sensation of satiety is provided.
  • the medical device being implantable and comprising a first member comprising a first stomach engager configured to engage a first portion of the stomach wall, and a second stomach engager portion configured to engage a second portion of the stomach wall.
  • the medical device further comprises a first stomach engager configured to engage a third portion of the stomach wall, and a second stomach engager portion configured to engage a fourth portion of the stomach wall.
  • the medical device further comprises a main portion, wherein the first and second members are operably connected to the main portion.
  • the medical device further comprises an operation device comprising an actuator, wherein the operation device is configured to displace the actuator, such that the actuator is configured to: in a first state, operate the first member for displacing the first stomach engager of the first member in relation to the second stomach engager of the first member, for stretching the stomach wall, and in a second state, operate the second member for displacing the first stomach engager of the second member in relation to the second stomach engager of the second member, for stretching the stomach wall.
  • the actuator is configured to in a first state, operate the first member for displacing the first stomach engager of the first member in away from the second stomach engager of the first member, for stretching a stomach wall portion between the first and second stomach engagers, and in a second state, operate the second member for displacing the first stomach engager of the second member in away from the second stomach engager of the second member, for stretching a stomach wall portion between the first and second stomach engagers.
  • the actuator is configured to: in a first state, operate the first member for displacing the first stomach engager of the first member towards the second stomach engager of the first member, for at least stretching a stomach wall portion between the first and second members, and in a second state, operate the second member for displacing the first stomach engager of the second member towards the second stomach engager of the second member, for at least stretching a stomach wall portion between the first and second members.
  • the first and second stomach engagers may be pivotably fixated to the main portion, and the first and second stomach engagers of the first member may be pivotably fixated to the main portion at a common point of pivot.
  • the first member is scissor-like and the first and second stomach engagers of the first member are operable in a scissors-like manner, such that the first and second stomach engagers can be displaced towards each other and away from each other by the operation of the handle-like portion of the scissor-like first member.
  • the operation device is configured to displace the actuator by a rotational movement.
  • the operation device is configured to displace the actuator by a combination of linear and rotational movement.
  • the actuator may in a first state be engaged with the first member and in a second state be engaged with the second member.
  • the operation device is configured to disengage the actuator from the first member by linear displacement of the actuator.
  • the medical device may further comprise a third member comprising: a first stomach engager configured to engage a fifth portion of the stomach wall, and a second stomach engager portion configured to engage a sixth portion of the stomach wall.
  • the operation device may be configured to displace the actuator, such that the actuator is configured to, in a third state, operate the third member for displacing the first stomach engager of the third member in relation to the second stomach engager of the third member, for stretching the stomach wall.
  • the medical device may further comprise a fourth member comprising: a first stomach engager configured to engage a seventh portion of the stomach wall, and a second stomach engager portion configured to engage an eight portion of the stomach wall.
  • the operation device may be configured to displace the actuator, such that the actuator is configured to, in a fourth state, operate the fourth member for displacing the first stomach engager of the fourth member in relation to the second stomach engager of the fourth member, for stretching the stomach wall.
  • the operation device may comprise a hydraulic operation device and the actuator comprise a hydraulic actuator, and the hydraulic actuator may comprise at least one hydraulic cylinder.
  • the hydraulic actuator comprises at least one flexible member comprising elevated and lowered portions.
  • the flexible member comprises at least one bellows.
  • the elevated and lowered portions are configured to enable the hydraulic actuator to be operable when fibrotic tissue is covering the elevated and lowered portions.
  • the operation device comprises an implantable pump configured to at least one of: provide hydraulic fluid for displacing the actuator by a rotational movement, provide hydraulic fluid for displacing the actuator by a linear movement, and provide hydraulic fluid for operating the actuator for displacing the first stomach engager in relation to the second stomach engager.
  • the implantable pump may be configured to be positioned at a remote location in relation to the main portion.
  • the operation device is operable by pressurized hydraulic fluid in a first direction and by an elastic element in an opposite direction.
  • the actuator is operable by pressurized hydraulic fluid in a first direction and by an elastic element in an opposite direction.
  • the operation device may further comprise a valve connected to the implantable pump.
  • the valve may be configured to: in a first state direct hydraulic fluid for displacing the actuator, and in a second state direct hydraulic fluid for operating the actuator for displacing the first stomach engager in relation to the second stomach engager.
  • the operation device comprises a mechanical operation device and the actuator comprises a mechanical actuator.
  • the mechanical actuator may comprise at least one electrical motor or solenoid.
  • the at least one electrical motor or solenoid may be configured to be positioned at a remote location in relation to the main portion.
  • the mechanical actuator may comprise at least one flexible member comprising elevated and lowered portions and the elevated and lowered portions may be configured to enable the mechanical actuator to be operable when fibrotic tissue is covering the elevated and lowered portions.
  • the electrical motor or solenoid is configured to at least one of: displace the actuator by a rotational movement, displace the actuator by a linear movement, and operate the actuator for displacing the first stomach engager in relation to the second stomach engager.
  • the stomach engagers may be configured to be invaginated by the stomach wall using stomach-to-stomach sutures or staplers.
  • the stomach engagers comprise at least one of: a fixation portion configured for fixation of the stomach engagers to tissue of the stomach wall using at least one of sutures and staplers, and a tissue growth promoting structure such that the stomach engagers can be fixated to the stomach wall by in-growth of fibrotic tissue.
  • the medical device may further comprise an energy storage unit for directly or indirectly energizing the medical device and/or a controller for controlling the operation device.
  • the controller may comprise a wireless transceiver for communicating wirelessly with a source external to the body of the patient.
  • the medical device further comprises at least one sensor, and the controller may be configured for receiving sensor input from the at least one sensor.
  • the senor is a sensor configured to sense a physical parameter of the medical device system.
  • the senor is a sensor configured to sense at least one of: a temperature of the medical device system, a parameter related to the power consumption of the medical device system, a parameter related to strain in the medical device system, a parameter related to a status of the energy storage unit, or a parameter related to the wireless transfer of energy from a source external to the body of the patient.
  • the senor may be a sensor configured to sense a physiological parameter of the patient.
  • the senor is a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, or pH.
  • the sensor configured to sense a parameter related to the patient swallowing comprises at least one of: a motility sensor, a acoustic sensor, an optical sensor, or a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller may be configured to transmit information based on sensor input to a source external to the body of the patient.
  • An implantable operation device for operating a body engaging portion of the implantable medical device is further provided, which may be one of the members described herein.
  • the implantable operation device comprising an electrical machine for transforming electrical energy to mechanical force, a flexible shaft for transferring the mechanical force to a body engaging portion, and a pre-tensioning device for creating a pre-tension in the flexible shaft.
  • the pre-tension eliminates slack end e.g. ensures that the flexible shaft remain threaded onto pulleys or the spools/drums at all time.
  • the pre-tensioning device may comprise a flexible element, which may comprise at least one of a spring and an elastic material.
  • the flexible shaft may be configured for transferring a linear force.
  • the flexible shaft may be a Bowden cable.
  • the electrical machine comprises an electrical motor or solenoid and the implantable operation device may further comprise a transmission for transforming the mechanical force created by electrical transforming device from a rotating mechanical force to a linear mechanical force.
  • the transmission may be configured for transforming the mechanical force created by electrical transforming device from a force having a first speed and a first strength to a force having a second lower speed and a second higher strength.
  • An implantable system comprising the implantable operation device according to any one of the preceding claims, and a body engaging portion configured to exert a force on a body portion of the patient, which may be a body engaging portion configured to engage the stomach wall of the patient for stretching the stomach wall such that satiety is created.
  • An implantable operation device for operating a body engaging portion of the implantable medical device is further provided, which may be one of the members described herein.
  • the implantable operation device comprising an electrical machine for transforming electrical energy to mechanical force, a transmission for transforming a mechanical force created by electrical transforming device from a force having a first speed and a first strength to a force having a second lower speed and a second higher strength.
  • the transmission comprises a first and second pulley, a flexible element configured to be placed around the first and second pulley, wherein the flexible element is configured to be pulled by the force having the first speed and first strength, causing the first and second pulley to displace in relation to each other with the force having the second lower speed and the second higher strength, thereby creating the transmission.
  • the transmission comprises a gun tackle.
  • the transmission comprises a luff or watch tackle.
  • the transmission comprises a double tackle.
  • the transmission comprises a gyn tackle.
  • the implantable operation device may further comprise a third pulley, and the third pully may be connected to the electrical machine and the flexible element may be configured to be placed around the third pulley such that operation of the electrical machine pulls the flexible element.
  • the flexible element is, or transitions into, a flexible shaft for transferring the mechanical force to a body engaging portion.
  • the flexible shaft may be configured for transferring a linear force.
  • the flexible shaft may be a Bowden cable.
  • the implantable operation device further comprising a pretensioning device for creating a pre-tension in the flexible element, which may be a pre-tensioning device comprising a flexible element which may comprise at least one of a spring and an elastic material.
  • the electrical machine comprises an electrical motor or solenoid. The electrical machine may be connected to a transmission for transforming the mechanical force created by electrical transforming device from a rotating mechanical force to a linear mechanical force.
  • the transmission may be configured for transforming the mechanical force created by the electrical machine from a force having a first speed and a first strength to a force having a second lower speed and a second higher strength.
  • An implantable system is further provided comprising the implantable operation device according to any one of the embodiments herein, and an implantable element configured to exert a force on a body portion of the patient.
  • An external device configured for communication with the implantable medical device according to any of the embodiments herein, when implanted in a patient, is further provided.
  • the external device comprises at least one first wireless transceiver configured for communication with the implantable medical device using a first network protocol, for determining a distance between the external device and the implantable medical device, and at least one second wireless transceiver configured for communication with the implantable medical device using a second network protocol, for transferring data between the external device and the implantable medical device.
  • the first wireless transceiver comprises an UWB transceiver.
  • the first wireless transceiver is configured for transcutaneous energy transfer for at least one of: powering an energy consuming component of the implantable medical device, and charging an implantable energy storage unit.
  • the second network protocol is a standard network protocol.
  • the second wireless transceiver comprises a Bluetooth transceiver.
  • the external device is further configured to communicate with a second external device using the at least one wireless transceiver.
  • the external device is configured for determining a distance between the external device and the implantable medical device by determining the RSSI.
  • the standard network protocol is one of, or a combination of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • a communication range of the first network protocol is less than a communication range of the second network protocol.
  • a frequency band of the first network protocol differs from a frequency band of the second network protocol.
  • the external device is configured to authenticate the implantable medical device if the determined distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the external device may be configured to allow the transfer of data between the external device and the implantable medical device after the implantable medical device has been authenticated.
  • the external device is a wearable external device.
  • the external device is a handset.
  • An implantable medical device configured for communication with an external device according to one of the embodiments herein is further provided.
  • the implantable medical device comprising at least one first wireless transceiver configured for communication with the external device using a first network protocol, for determining a distance between the external device and the implantable medical device, and at least one second wireless transceiver configured for communication with the external device using a second network protocol, for transferring data between the external device and the implantable medical device.
  • the first wireless transceiver comprises an UWB transceiver.
  • the first wireless transceiver is configured for transcutaneous energy transfer for at least one of: powering an energy consuming component of the implantable medical device, and charging an implantable energy storage unit.
  • the second network protocol is a standard network protocol.
  • the second wireless transceiver comprises a Bluetooth transceiver.
  • the implantable medical device is further configured to communicate with a second external device using said at least one wireless transceiver.
  • the implantable medical device is configured for determining a distance between the external device and the implantable medical device by determining the RSSI.
  • the standard network protocol is one of, or a combination of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the communication range of the first network protocol may be less than the communication range of the second network protocol.
  • the frequency band of the first network protocol may differ from a frequency band of the second network protocol.
  • the implantable medical device is configured to authenticate the external device if the determined distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the implantable medical device may be configured to allow the transfer of data between the implantable medical device and the external device after the external device has been authenticated.
  • An external device configured for communication with an implantable medical device according to any one of the embodiments disclosed herein is further provided.
  • the external device comprising a wireless communication unit configured for wireless transmission of control commands to the implantable medical device and configured for wireless communication with a display device, and a computing unit configured for running a control software for creating the control commands for the operation of the implantable medical device.
  • the computing unit may be configured to transmit a control interface to a display device configured to display the control interface to a user, receive user input from the display device, and transform the user input into the control commands for wireless transmission to the implantable medical device.
  • the wireless communication unit comprises a wireless transceiver for wireless transmission of control commands to the implantable medical device, and wireless transmission of the control interface to the display device.
  • the wireless communication unit comprises a first wireless transceiver for wireless transmission of control commands to the implantable medical device, and a second wireless transceiver for wireless transmission of the control interface to the display device.
  • the wireless communication unit may in one embodiment be configured for wireless communication with the display device using a standard network protocol.
  • the wireless communication unit is configured for wireless communication with the implantable medical device using a proprietary network protocol.
  • the wireless communication unit may comprise a Bluetooth transceiver, which may be comprised in one of the first and second wireless transceiver.
  • the wireless communication unit comprises a UWB transceiver, which may be comprised in one of the first and second wireless transceiver.
  • the wireless communication unit may comprise at least one first wireless transceiver configured for communication with the implantable medical device using a first network protocol, for determining a distance between the external device and the implantable medical device, and at least one second wireless transceiver configured for communication with the implantable medical device using a second network protocol, for transferring data between the external device and the implantable medical device.
  • the first wireless transceiver is configured for transcutaneous energy transfer for at least one of: powering an energy consuming component of the implantable medical device, and charging an implantable energy storage unit.
  • the standard network protocol is one of, or a combination of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the communication range of the first wireless transceiver may be less than a communication range of the second wireless transceiver
  • the frequency band of the first network protocol may differ from a frequency band of the second network protocol.
  • the external device is configured to authenticate the implantable medical device if a distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the external device is configured to be authenticated by the implantable medical device if a distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the external device is configured to authenticate the display device if a distance between the external device and the display device is less than a predetermined threshold value.
  • the external device is configured to be authenticated by the implantable medical device if a distance between the external device and the display device is less than a predetermined threshold value.
  • the external device may be configured to allow the transfer of data between the external device and the implantable medical device, and/or the external device and the display device, on the basis of the authentication.
  • the computing unit is configured to encrypt at least one of the control interface and the control commands.
  • a display device for communication with an external device for communication with an implantable medical device is further provided.
  • the display device comprises a wireless communication unit configured for wirelessly receiving an implant control interface from the external device and configured for wirelessly transmitting implant control user input to the external device.
  • the display device further comprising a display for displaying the received implant control interface, and an input device for receiving implant control input from the user.
  • the display device further comprises an auxiliary wireless communication unit configured to be disabled to enable at least one of: wirelessly receiving the implant control interface from the external device, and wirelessly transmitting implant control user input to the external device.
  • the wireless communication unit is configured for wireless communication with the external device using a standard network protocol.
  • the wireless communication unit is configured for wireless communication with the external device using a proprietary network protocol.
  • the wireless communication unit comprises a Bluetooth transceiver.
  • the wireless communication unit comprises a UWB transceiver.
  • the standard network protocol is one of, or a combination of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the communication range of the wireless communication unit of the display device may be less than a communication range of the auxiliary wireless communication unit.
  • the display device is configured to authenticate the external device if a distance between the display device and the external device is less than a predetermined threshold value.
  • the display device is configured to be authenticated by the external device if a distance between the display device and the external device is less than a predetermined threshold value.
  • the display device is configured to allow the transfer of data between the display device and the external device on the basis of the authentication.
  • the display device may be a wearable external device or a handset.
  • a communication system for enabling communication between a display device and an implantable medical device comprising a display device, a server, and an external device.
  • the display device comprises a wireless communication unit configured for wirelessly receiving an implant control interface from the server, the implant control interface being provided by the external device, the wireless communication unit further being configured for wirelessly transmitting implant control user input to the server, destined for the external device, a display for displaying the received implant control interface, and an input device for receiving implant control input from the user.
  • the server of the communication system comprises: a wireless communication unit configured for wirelessly receiving an implant control interface from the external device and wirelessly transmitting the implant control interface to the display device, the wireless communication unit further being configured for wirelessly receiving implant control user input from the display device and wirelessly transmitting the implant control user input to the external device.
  • the external device of the communication system comprises a wireless communication unit configured for wireless transmission of control commands to the implantable medical device and configured for wireless communication with the server, and a computing unit configured for: running a control software for creating the control [000439] commands for the operation of the implantable medical device, transmit a control interface to the server, destined for the display device, receive implant control user input generated at the [000440] display device, from the server, and transform the user input into the control commands for wireless transmission to the implantable medical device.
  • the computing unit of the communication system is configured to encrypt at least one of the control interface and the control commands.
  • the display device is configured to encrypt the user input.
  • the server is configured to encrypt at least one of the user input received from the display device and the control interface received from the external device. [000444]
  • the computing unit is configured to encrypt the control interface and the display device is configured to decrypt the encrypted control interface.
  • the server is configured to act as a router, transferring the encrypted control interface from the external device to the display device without decryption.
  • a display device for communication with an external device for communication with an implantable medical device comprising a wireless communication unit, a display, and an input device for receiving implant control input from the user.
  • the display device is configured to run a first application for wireless communication with a server, and to run a second application for wireless communication with the external device for transmission of the implant control input to the external device for the communication with the implantable medical device, wherein the second application is configured to be accessed through the first application.
  • the display device may comprise a first log-in function and a second log-in function, and wherein the first log-in function gives the user access to the first application and wherein the first and second log-in function in combination gives the user access to the second application.
  • the first log-in is a PIN-based log-in.
  • At least one of the first and second log-in is a log-in based on a biometric input or a hardware key.
  • the display device further comprises an auxiliary wireless communication unit, and the auxiliary wireless communication unit is configured to be disabled to enable wireless communication with the external device.
  • the display device is configured to wirelessly receive an implant control interface from the external device to be displayed on the display.
  • the wireless communication unit is configured for wireless communication with the external device using a standard network protocol.
  • the wireless communication unit is configured for wireless communication with the external device using a proprietary network protocol.
  • the wireless communication unit is configured for wireless communication with the external device using a first network protocol and with the server using a second network protocol.
  • the wireless communication unit is configured for wireless communication with the external device using a first frequency band and with the server using a second frequency band.
  • the wireless communication unit comprises a Bluetooth transceiver.
  • the wireless communication unit comprises a UWB transceiver.
  • the standard network protocol is one of, or a combination of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the communication range of the wireless communication unit is less than a communication range of the auxiliary wireless communication unit.
  • the wireless communication unit comprises a first wireless transceiver for communication with the external device and a second wireless transceiver for communication with the server.
  • the second wireless transceiver may be configured to be disabled to enable wireless communication using the first wireless transceiver.
  • the display device is configured to authenticate the external device if a distance between the display device and the external device is less than a predetermined threshold value, and the display device is configured to be authenticated by the external device if a distance between the display device and the external device is less than a predetermined threshold value.
  • the display device is configured to allow the transfer of data between the display device and the external device on the basis of the authentication.
  • the display device may be a wearable external device or a handset.
  • the second application may be configured to receive data related to a parameter of the implanted medical device.
  • the second application is configured to receive data related to a sensor value received from the implanted medical device.
  • the second application is configured to receive data related to a parameter related to at least one of: a battery status, a temperature, a time, or an error.
  • the display device is configured to encrypt the user input.
  • the display is configured to encrypt the user input for decryption by the implantable medical device.
  • the display device is configured to decrypt the control interface received from the external device, for displaying the control interface on the display.
  • at least one of the first and second application is configured to receive data from an auxiliary external device and present the received data to the user.
  • At least one of the first and second application may be configured to receive data from an auxiliary external device comprising a scale for determining the weight of the user.
  • At least one of the first and second application may be configured to receive data related to the weight of the user from an auxiliary external device comprising a scale.
  • the display device is configured to: wirelessly transmit the data related to the weight of the user to the external device, or wirelessly transmit an instruction derived from the data related to the weight of the user, or wirelessly transmit an instruction derived from a combination of the data related to the weight of the user and the implant control input received from the user.
  • a communication system for enabling communication between a display device and an implantable medical device comprises a display device, a server, and an external device.
  • the display device comprises: a wireless communication unit configured for wirelessly receiving an implant control interface from the external device, the wireless communication unit further being configured for wirelessly transmitting implant control user input to the external device.
  • the display device further comprises a display for displaying the received implant control interface, and an input device for receiving implant control input from the user, wherein the display device is configured to run a first application for wireless communication with the server, and to run a second application for wireless communication with the external device for transmission of the implant control input to the external device for the communication with the implantable medical device.
  • the external device comprises a wireless communication unit configured for wireless transmission of control commands based on the implant control input to the implantable medical device and configured for wireless communication with the display device.
  • the display device comprises a first log-in function and a second log-in function, and wherein the first log-in function gives the user access to the first application and wherein the first and second log-in function in combination gives the user access to the second application.
  • the second application may be configured to receive data related to a parameter of the implanted medical device, and the second application may be configured to receive data related to a sensor value received from the implanted medical device.
  • the second application is configured to receive data related to a parameter related to at least one of: a battery status, a temperature, a time, or an error.
  • the display device is configured to encrypt the user input.
  • the display is configured to encrypt the user input for decryption by the implantable medical device.
  • the external device is configured to act as a router, transferring the encrypted user input from the display device to the implantable medical device without decryption.
  • the external device is configured to encrypt at least one of the control interface and the control commands.
  • the external device is configured to encrypt the control interface and wherein the display device is configured to decrypt the encrypted control interface.
  • a computer program product configured to run in a display device comprising a wireless communication unit, a display for displaying the received implant control interface, and an input device for receiving implant control input from a user is further provided.
  • the computer program product comprising a first application for communication with a server, and a second application for communication with an external device for transmission of the implant control input to the external device for the communication with an implantable medical device, wherein the second application is configured to be accessed through the first application.
  • the computer program product further comprises a first log-in function, and a second log-in function, wherein the first log-in function gives the user access to the first application and the first and second log-in function in combination gives the user access to the second application.
  • the second application is configured to receive data related to a parameter of the implanted medical device.
  • the second application is configured to receive data related to a sensor value received from the implanted medical device.
  • the second application is configured to receive data related to a parameter related to at least one of: a battery status, a temperature, a time, or an error.
  • a communication system for enabling communication between a display device, an external device, a server and an implantable medical device comprising: a server, a display device, an external device, and an implantable medical device.
  • the display device comprises: a wireless communication unit for wirelessly communicating with at least one of the external device and the server, a display, and an input device for receiving input from the user.
  • the external device comprises: a wireless communication unit configured for wireless transmission of control commands to the implantable medical device and configured for wireless communication with at least one of the display device and the server.
  • the server comprises: a wireless communication unit configured for wireless communication with at least one of the display device and the external device.
  • the implantable medical device comprises: a wireless communication unit configured for wireless communication with the external device.
  • the implantable medical device comprises an encryption unit which is configured to encrypt data destined for the server, transmit the data to the server via the external device, wherein the external device acts as a router transferring the data without full decryption, or the implantable medical device comprises an encryption unit and is configured to: encrypt data destined for the display device, transmit the data to the display device via the external device, wherein the external device acts as a router transferring the data without full decryption, or the server comprises an encryption unit and is configured to: encrypt data destined for the implantable medical device, transmit the data to the implantable medical device via the external device, wherein the external device acts as a router transferring the data without full decryption, or the server comprises an encryption unit and is configured to: encrypt data destined for the implantable medical device, transmit the data to the implantable medical device via the display device and the external device, wherein the display device and the external device acts as a router transferring the data without full decryption, or the display device comprises an encryption unit and is configured to
  • the display device is configured to wirelessly receive an implant control interface from the external device to be displayed on the display.
  • At least two of: the wireless communication unit of the server, the wireless communication unit of the display device, the wireless communication unit of the external device, and the wireless communication unit of the implantable medical device - is configured for wireless communication using a standard network protocol.
  • the at least two of: the wireless communication unit of the server, the wireless communication unit of the display device, the wireless communication unit of the external device, and the wireless communication unit of the implantable medical device - is configured for wireless communication using a proprietary network protocol.
  • the wireless communication unit of the external device is configured to: use a first network protocol for communication with the implantable medical device and use a second network protocol for communication with the server, or use a first network protocol for communication with the implantable medical device and use a second network protocol for communication with the display device.
  • the wireless communication unit of the external device is configured to: use a first frequency band for communication with the implantable medical device and use a second frequency band for communication with the server, or use a first frequency band for communication with the implantable medical device and use a second frequency band for communication with the display device.
  • the wireless communication unit of the display device is configured to use a first network protocol for communication with the external device and use a second network protocol for communication with the server.
  • the wireless communication unit of the display device is configured to use a first frequency band for communication with the external device and use a second frequency band for communication with the server.
  • the wireless communication unit of the server is configured to use a first network protocol for communication with the external device and use a second network protocol for communication with the display device.
  • the wireless communication unit of the server is configured to use a first frequency band for communication with the external device and use a second frequency band for communication with the display device.
  • the wireless communication unit of at least one of the server, the display device, the external device, and the implantable medical device comprises a Bluetooth transceiver.
  • the wireless communication unit of at least one of the server, the display device, the external device, and the implantable medical device comprises a UWB transceiver.
  • the standard network protocol is one from the list of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and a GSM type protocol.
  • the wireless communication unit of the external device comprises a first wireless transceiver for wireless communication with the implantable medical device, and a second wireless transceiver for wireless communication with the server, and wherein the second wireless transceiver has a longer effective range than the first wireless transceiver.
  • the wireless communication unit of the external device comprises a first wireless transceiver for wireless communication with the implantable medical device, and a second wireless transceiver for wireless communication with the display device, and wherein the second wireless transceiver has a longer effective range than the first wireless transceiver.
  • the wireless communication unit of the display device comprises a first wireless transceiver for wireless communication with the external device, and a second wireless transceiver for wireless communication with the server, and wherein the second wireless transceiver has a longer effective range than the first wireless transceiver.
  • the second wireless transceiver has an effective range being one of: 2 times, 4 times, 8 times 20 times, 50 times or 100 times longer than the first wireless transceiver.
  • the second wireless transceiver is configured to be disabled to enable wireless communication using the first wireless transceiver.
  • the display device is configured to authenticate the external device if a distance between the display device and the external device is less than a predetermined threshold value
  • the display device is configured to be authenticated by the external device if a distance between the display device and the external device is less than a predetermined threshold value, [000510] the display device is configured to authenticate the implantable medical device if a distance between the display device and the implantable medical device is less than a predetermined threshold value,
  • the display device is configured to be authenticated by the implantable medical device if a distance between the display device and the implantable medical device is less than a predetermined threshold value
  • the external device is configured to authenticate the display device if a distance between the external device and the display device is less than a predetermined threshold value
  • the external device is configured to be authenticated by the display device if a distance between the external device and the display device is less than a predetermined threshold value, [000514] the external device is configured to authenticate the implantable medical device if a distance between the external device and the implantable medical device is less than a predetermined threshold value, and
  • the external device is configured to be authenticated by the implantable medical device if a distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the display device may be configured to allow the transfer of data between the display device and the external device on the basis of the authentication.
  • the external device is configured to allow the transfer of data between the display device and the external device on the basis of the authentication.
  • the external device is configured to allow the transfer of data between the external device and the implantable medical device on the basis of the authentication.
  • the display device is a wearable external device or a handset.
  • the data encrypted by the implantable medical device is related to at least one of: a battery status, a temperature, a time, or an error.
  • a server for use in the communication system according to any one of the embodiments above is further provided, claims 1 - 24.
  • a display device for use in the communication system according to any one of the embodiments above is further provided.
  • An external device for use in the communication system according to any one of the embodiments above is further provided.
  • An implantable medical device for use in the communication system according to any one of the embodiments above is further provided.
  • Medical devices designed to be implanted in a patient's body, are typically operated by means of electrical power.
  • Such medical devices include electrical and mechanical stimulators, motors, pumps, etc, which are designed to support or stimulate various body functions.
  • Electrical power can be supplied to such an implanted medical device from a likewise implanted battery or from an external energy source that can supply any needed amount of electrical power intermittently or continuously without requiring repeated surgical operations.
  • An implanted energy receiver or other implanted devices required for the operation of an implanted medical device must in some way be located in the patient's body in a secure and convenient way. It is often the case that the implanted device must be located close to the patient's skin in order to keep the distance between an external device, such as an energy transmitter, and the implanted device to a minimum. In practice, this means subcutaneous placement of the implanted device.
  • an remote unit configured to be held in position by a tissue portion of a patient, the remote unit comprising: a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion extending between the first and second sides of the tissue portion, the connecting portion having a third cross
  • the connecting portion comprises a flange comprising the fourth cross-sectional area, such that the flange is prevented from travelling through the hole in the tissue portion in a direction perpendicular to the first, second and third planes.
  • the flange protrudes in a direction parallel to the first, second, third and fourth planes, and perpendicular to a central extension of the connecting portion.
  • the flange comprises the third surface configured to engage the first tissue surface of the first side of the tissue portion.
  • the connecting portion comprises at least one protruding element comprising the fourth cross-sectional area, such that the at least one protruding element is prevented from travelling through the hole in the tissue portion, such that the second portion and the connecting portion can be held in position by the tissue portion of the patient also when the first portion is disconnected from the connecting portion.
  • the at least one protruding element protrudes in a direction parallel to the first, second, third and fourth planes, and perpendicular to a central extension of the connecting portion.
  • the at least one protruding element comprises the third surface configured to engage the first tissue surface of the first side of the tissue portion.
  • the connecting portion comprises at least two protruding elements comprising the fourth cross-sectional area.
  • the at least two protruding elements are symmetrically arranged about a central axis of the connecting portion.
  • the at least two protruding elements are asymmetrically arranged about a central axis of the connecting portion.
  • at least one of the first, second and third surfaces comprises at least one of ribs, barbs, hooks, a friction enhancing surface treatment, and a friction enhancing material, to facilitate the remote unit being held in position by the tissue portion.
  • the connecting portion comprises a hollow portion.
  • the hollow portion provides a passage between the first and second portions.
  • the first portion is detachably connected to the connecting portion by at least one of a mechanical connection and a magnetic connection.
  • the first portion is detachably connected to the connecting portion by at least one of threads and corresponding grooves, a screw, a self-locking element, a twist and lock fitting, and a spring-loaded locking mechanism.
  • the at least one protruding element has a height in a direction perpendicular to the fourth plane being less than a height of the first portion in said direction.
  • the at least one protruding element has a height in said direction perpendicular to the fourth plane being less than half of said height of the first portion in said direction.
  • the at least one protruding element has a height in said direction perpendicular to the fourth plane being less than a quarter of said height of the first portion in said direction.
  • the at least one protruding element has a height in said direction perpendicular to the fourth plane being less than a tenth of said height of the first portion in said direction.
  • the at least one protruding element has a diameter in the fourth plane being one of: less than a diameter of the first portion in the first plane, equal to a diameter of the first portion in the first plane, and larger than a diameter of the first portion in the first plane.
  • the at least one protruding element has a cross-sectional area in the fourth plane being one of: less than a cross-sectional area of the first portion in the first plane, equal to a cross-sectional area of the first portion in the first plane, and larger than a cross-sectional area of the first portion in the first plane.
  • the at least one protruding element has a height in said direction perpendicular to the fourth plane being less than half of a height of the connecting portion in said direction.
  • the at least one protruding element has a height in said direction perpendicular to the fourth plane being less than a quarter of said height of the connecting portion in said direction.
  • the at least one protruding element has a height in said direction perpendicular to the fourth plane being less than a tenth of said height of the connecting portion in said direction.
  • an remote unit configured to be held in position by a tissue portion of a patient, the remote unit comprising: a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion extending between the first and second sides of the tissue portion, the connecting portion having a third cross-sectional area in a third plane and being configured to connect the first portion to the second portion, wherein: the first, second, and third planes are
  • the connecting interface between the connecting portion and the second portion is excentric, with respect to the second portion, in a first direction, but not in a second direction being perpendicular to the first direction.
  • the connecting interface between the connecting portion and the second portion is excentric, with respect to the second portion, in a first direction and in a second direction being perpendicular to the first direction.
  • the first direction and second direction are parallel to the second plane.
  • the second portion has a first end and a second end opposing the first end, wherein the second portion has a length between the first and second end.
  • the first end and second end are separated in a direction parallel to the second plane.
  • the second portion is curved along the length.
  • the second portion is curved in said first direction and said second direction being perpendicular to the first direction.
  • the first and second ends comprise an elliptical point respectively.
  • the first and second ends comprise a hemispherical end cap respectively.
  • the second portion has at least one circular cross-section along the length between the first and second end.
  • the second portion has at least one oval cross-section along the length between the first and second end.
  • the second portion has at least one elliptical cross-section along the length between the first and second end.
  • the second portion has said length in a direction being different to a central extension of the connecting portion.
  • the second portion has a proximal region, an intermediate region, and a distal region.
  • the proximal region extends from the first end to an interface between the connecting portion and the second portion
  • the intermediate region is defined by the connecting interface between the connecting portion and the second portion
  • the distal region extends from the interface between the connecting portion and the second portion to the second end.
  • the proximal region is shorter than the distal region with respect to the length of the second portion.
  • the proximal region and the intermediate region together are shorter than the distal region with respect to the length of the second portion.
  • the proximal region and the distal region comprises the second surface configured to engage the second surface of the second side of the tissue portion.
  • the second portion has a length x and a width y along respective length and width directions being perpendicular to each other and substantially parallel to the second plane, wherein the connecting interface between the connecting portion and the second portion is contained within a region extending from x>0 to x ⁇ x/2 and/or y>0 to y ⁇ y/2, x and y and 0 being respective end points of the second portion along said length and width directions.
  • the second portion is tapered from the first end to the second end.
  • the second portion is tapered from each of the first end and second end towards the intermediate region of the second portion.
  • the first portion has a maximum dimension being in the range of 10 to 40 mm, such as in the range of 10 to 30 mm, such as in the range of 15 to 25 mm.
  • the first portion has a diameter being in the range of 10 to 40 mm, such as in the range of 10 to 30 mm, such as in the range of 15 to 25 mm.
  • the connecting portion has a maximum dimension in the third plane in the range of 2 to 20 mm, such as in the range of 2 to 15 mm, such as in the range of 5 to 10 mm.
  • the second portion has a maximum dimension being in the range of 30 to 90 mm, such as in the range of 30 to 70 mm, such as in the range of 35 to 60 mm.
  • the first portion has one or more of a spherical shape, an ellipsoidal shape, a polyhedral shape, an elongated shape, and a flat disk shape.
  • the connecting portion has one of an oval cross-section, an elongated cross-section, and a circular cross-section, in a plane parallel to the third plane.
  • the distal region is configured to be directed downwards in a standing patient.
  • the first portion comprises a proximal region extending from an first end to an interface between the connecting portion and the first portion, an intermediate region defined by an connecting interface between the connecting portion and the first portion, and a distal region extending from the interface between the connecting portion and the first portion to a second end of the first portion.
  • the first portion has a first height
  • the second portion has a second height, both heights being in a direction perpendicular to the first and second planes, wherein the first height is smaller than the second height.
  • the first height is less than 2/3 of the second height, such as less than 1/2 of the second height, such as less than 1/3 of the second height.
  • the second end of the second portion comprises connections for connecting to an implant being located in a caudal direction from a location of the remote unit in the patient.
  • the first end of the second portion comprises connections for connecting to an implant being located in a cranial direction from a location of the remote unit in the patient.
  • an remote unit configured to be held in position by a tissue portion of a patient, the remote unit comprising: a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion extending between the first and second sides of the tissue portion, the connecting portion has a third cross-sectional area in a third plane and is configured to connect the first portion to the second portion, wherein: the first, second and third planes are parallel
  • the first cross-sectional distance of the first cross-sectional area and the first cross-sectional distance of the second cross-sectional area are rotationally displaced in relation to each other with an angle exceeding 60° to facilitate insertion of the second portion through the hole in the tissue portion.
  • the first cross-sectional distance of the first cross-sectional area and the first cross-sectional distance of the second cross-sectional area are substantially perpendicular to each other to facilitate insertion of the second portion through the hole in the tissue portion.
  • the first cross-sectional distance of the first cross-sectional area and the first cross-sectional distance of the second cross-sectional area are rotationally displaced in relation to each other with an angle exceeding 45° and being less than 135°.
  • the cross-sectional area of the first portion is elongated.
  • the cross-sectional area of the second portion is elongated.
  • the connecting portion is connected eccentrically to the second portion.
  • the first cross-sectional distance of the second portion is divided into a first, second and third equal length-portions, and wherein the connecting portion is connected to the second portion along the first length-portion of the first cross-sectional distance.
  • the first cross-sectional area of the first portion is elongated.
  • the second cross-sectional area of the second portion is elongated.
  • the first portion comprises a first wireless energy receiver configured to receive energy transmitted wirelessly from an external wireless energy transmitter.
  • the first portion comprises an internal wireless energy transmitter.
  • the second portion comprises a second wireless energy receiver.
  • the first portion comprises a first energy storage unit.
  • the second portion comprises a second energy storage unit.
  • At least one of the first and second energy storage unit is a solid-state battery.
  • the solid-state battery is a thionyl-chloride battery.
  • the first wireless energy receiver is configured to receive energy transmitted wirelessly by the external wireless energy transmitter, and store the received energy in the first energy storage unit
  • the internal wireless energy transmitter is configured to wirelessly transmit energy stored in the first energy storage unit to the second wireless energy receiver
  • the second wireless energy receiver is configured to receive energy transmitted wirelessly by the internal wireless energy transmitter and store the received energy in the second energy storage unit.
  • the first portion comprises a first controller comprising at least one processing unit.
  • the second portion comprises a second controller comprising at least one processing unit.
  • At least one of the first and second controller is connected to a wireless transceiver for communicating wirelessly with an external device.
  • the first controller is connected to a first wireless communication receiver in the first portion for receiving wireless communication from an external device, and the first controller is connected to a first wireless communication transmitter in the first portion for transmitting wireless communication to a second wireless communication receiver in the second portion.
  • the second controller is connected to the second wireless communication receiver for receiving wireless communication from the first portion.
  • the first wireless energy receiver comprises a first coil and the internal wireless energy transmitter comprises a second coil.
  • the first portion comprises a combined coil, wherein the combined coil is configured to receive energy wirelessly from an external wireless energy transmitter, and transmit energy wirelessly to the second wireless receiver of the second portion.
  • the remote unit further comprises a housing configured to enclose at least the first portion, and wherein a first portion of the housing is made from titanium and a second portion of the housing is made from a ceramic material.
  • the portion of the housing made from a ceramic material comprises at least one coil embedded in the ceramic material.
  • the remote unit further comprises a housing configured to enclose at least the second portion, and wherein a first portion of the housing is made from titanium and a second portion of the housing is made from a ceramic material.
  • the portion of the housing made from a ceramic material comprises at least one coil embedded in the ceramic material.
  • an remote unit configured to be held in position by a tissue portion of a patient, the remote unit comprising: a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion extending between the first and second sides of the tissue portion, the connecting portion having a third cross-sectional area in a third plane and being configured to connect the first portion to the second portion, wherein: the first, second, and third planes are parallel
  • the senor is a sensor configured to sense a physical parameter of the remote unit.
  • the senor is a sensor configured to sense at least one of: a temperature of the remote unit or of a body engaging portion, a parameter related to the power consumption of the remote unit or of a body engaging portion, a parameter related to a status of at least one of the first and second energy storage unit, a parameter related to the wireless transfer of energy from a source external to the body of the patient, and a hydraulic pressure.
  • the senor is a sensor configured to sense a physiological parameter of the patient.
  • the sensor is a sensor configured to sense at least one of: a parameter related to the patient swallowing, a local temperature, a systemic temperature, blood saturation, blood oxygenation, blood pressure, a parameter related to an ischemia marker, and pH.
  • the sensor configured to sense a parameter related to the patient swallowing comprises at least one of: a motility sensor, a acoustic sensor, an optical sensor, and a strain sensor.
  • the sensor configured to sense pH is configured to sense the acidity in the stomach.
  • the controller is configured to transmit information based on sensor input to a device external to the body of the patient.
  • the second portion comprises at least a portion of an operation device for operating an implantable body engaging portion.
  • the second portion comprises at least one electrical motor.
  • the second portion comprises a transmission configured to reduce the speed and increase the force of the movement generated by the electrical motor.
  • the transmission is configured to transfer a week force with a high speed into a stronger force with lower speed.
  • the transmission is configured to transfer a rotating force into a linear force.
  • the transmission comprises a gear system.
  • the second portion comprises a magnetic coupling for transferring mechanical work from the electrical motor through one of: a barrier separating a first chamber of the second portion from a second chamber of the second portion, a housing enclosing at least the second portion.
  • the second portion comprises at least one hydraulic pump.
  • the hydraulic pump comprises a pump comprising at least one compressible hydraulic reservoir.
  • the remote unit further comprises a capacitor connected to at least one of the first and second energy storage unit and connected to the electrical motor, wherein the capacitor is configured to: be charged by at least one of the first and second energy storage units, and provide the electrical motor with electrical power.
  • At least one of the first and second portion comprises a sensation generator adapted to generate a sensation detectable by a sense of the patient.
  • the second portion comprises a force transferring element configured to mechanically transfer force from the second portion to an implanted body engaging portion.
  • the second portion comprises a force transferring element configured to hydraulically transfer force from the second portion to an implanted body engaging portion.
  • the second portion comprises at least one lead for transferring electrical energy and/or information from the second portion to an implanted body engaging portion.
  • the first portion comprises an injection port for injecting fluid into the first portion.
  • the connecting portion comprises a conduit for transferring a fluid from the first portion to the second portion.
  • the conduit is arranged to extend through the hollow portion of the connecting portion.
  • the second portion comprises a first and a second chamber separated from each other, wherein the first chamber comprises a first liquid and the second chamber comprises a second liquid, and wherein the second liquid is a hydraulic liquid configured to transfer force to an implantable element configured to exert force on the body portion of the patient.
  • a wall portion of the first chamber is resilient to allow an expansion of the first chamber.
  • the second portion comprises a first hydraulic system in fluid connection with a first hydraulically operable implantable element configured to exert force on the body portion of the patient, and a second hydraulic system in fluid connection with a second hydraulically operable implantable element configured to exert force on the body portion of the patient, wherein the first and second hydraulically operable implantable elements are adjustable independently from each other.
  • the first hydraulic system comprises a first hydraulic pump and the second hydraulic systems comprises a second hydraulic pump.
  • each of the first and second hydraulic systems comprises a reservoir for holding hydraulic fluid.
  • the implantable energized medical further comprises a first pressure sensor configured to sense a pressure in the first hydraulic system, and a second pressure sensor configured to sense a pressure in the second hydraulic system.
  • the first surface is configured to engage the first tissue surface of the first side of the tissue portion.
  • the first, second and third planes are parallel to a major extension plane of the tissue.
  • an remote unit configured to be held in position by a tissue portion of a patient, the remote unit comprising: a first portion configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, a second portion configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and comprising a second surface configured to engage a second tissue surface of the second side of the tissue portion, and a connecting portion configured to be placed through a hole in the tissue portion extending between the first and second sides of the tissue portion, the connecting portion having a third cross-sectional area in a third plane and being configured to connect the first portion to the second portion, wherein: the first, second, and third planes are
  • the first portion comprises a first wireless energy receiver configured to receive energy transmitted wirelessly from an external wireless energy transmitter.
  • the first portion comprises a first wireless communication receiver.
  • the first portion comprises a coil embedded in a ceramic material, hereinafter referred to as a first coil.
  • the first wireless energy receiver comprises the first coil.
  • the first wireless communication receiver comprises the first coil.
  • the first portion comprises a distal end and a proximal end with respect to the connecting portion, along a direction perpendicular to the first plane.
  • the first coil is arranged at the distal end of the first portion.
  • the first portion comprises an internal wireless energy transmitter.
  • the first portion comprises a first wireless communication transmitter.
  • the first portion comprises a coil embedded in a ceramic material, hereinafter referred to as a second coil.
  • the internal wireless energy transmitter comprises the second coil.
  • the first wireless communication transmitter comprises the second coil.
  • the second coil is arranged at the proximal end of the first portion.
  • the first wireless energy receiver and the internal wireless energy transmitter comprises a single coil embedded in a ceramic material.
  • the first wireless communication receiver and the first wireless communication transmitter comprises a single coil embedded in a ceramic material.
  • the first wireless energy receiver, the internal wireless energy transmitter, the first wireless communication receiver, and the internal wireless communication transmitter comprises a single coil embedded in a ceramic material.
  • the second portion comprises a second wireless energy receiver.
  • the second portion comprises a coil embedded in a ceramic material, hereinafter referred to as a third coil, wherein the second wireless energy receiver comprises the third coil.
  • the second portion comprises a distal end and a proximal end with respect to the connecting portion, along a direction perpendicular to the first plane.
  • the third coil is arranged at the proximal end of the second portion.
  • the first portion comprises a first energy storage unit.
  • the second portion comprises a second energy storage unit.
  • the first wireless energy receiver is configured to receive energy transmitted wirelessly by the external wireless energy transmitter, and store the received energy in the first energy storage unit
  • the internal wireless energy transmitter is configured to wirelessly transmit energy stored in the first energy storage unit to the second wireless energy receiver
  • the second wireless energy receiver is configured to receive energy transmitted wirelessly by the internal wireless energy transmitter and store the received energy in the second energy storage unit.
  • the first energy storage unit is configured to store less energy than the second energy storage unit, and configured to be charged faster than the second energy storage unit.
  • the first energy storage unit has lower energy density than the second energy storage unit.
  • the remote unit further comprises a housing configured to enclose at least the first portion, and wherein a first portion of the housing is made from titanium and a second portion of the housing is made from a ceramic material.
  • the housing made from a ceramic material comprises the at least one coil embedded in the ceramic material.
  • the remote unit further comprises a housing configured to enclose at least the second portion, and wherein a first portion of the housing is made from titanium and a second portion of the housing is made from a ceramic material.
  • the portion of the housing made from a ceramic material comprises the at least one coil embedded in the ceramic material.
  • the first, second and third planes are parallel to a major extension plane of the tissue.
  • the connecting portion further comprises a fourt cross-sectional area in a fourth plane, wherein the fourt plane is parallel to the first, second and third planes, and wherein the third cross-sectional area is smaller than the fourth cross-sectional area.
  • the connecting portion comprises a protruding element comprising the fourth cross-sectional area.
  • the fourth plane is parallel to a major extension plane of the tissue.
  • a connecting interface between the connecting portion and the second portion is excentric with respect to the second portion.
  • an implantable device for exerting a force on a body portion of a patient comprising: an remote unit and an implantable element configured to exert a force on a body portion of the patient.
  • the implantable element configured to exert a force on a body portion of the patient is an implantable hydraulic constriction device.
  • the implantable hydraulic constriction device is configured for constricting a luminary organ of the patient.
  • the implantable hydraulic constriction device comprises an implantable hydraulic constriction device for constricting an intestine of the patient.
  • the implantable hydraulic constriction device comprises an implantable hydraulic constriction device for constricting a colon or rectum of the patient.
  • the implantable hydraulic constriction device comprises an implantable hydraulic constriction device for constricting the intestine at a region of a stoma of the patient.
  • the implantable hydraulic constriction device comprises an implantable hydraulic constriction device for constricting a blood vessel of the patient.
  • the implantable hydraulic constriction device for constricting a blood vessel of the patient is configured to constrict the venous blood flow leading from an erectile tissue for promoting the engorgement of the erectile tissue.
  • the implantable hydraulic constriction device comprises an implantable hydraulic constriction device for constricting a vas deference of the patient.
  • the implantable element configured to exert a force on a body portion of the patient is an implantable element for actively emptying the urinary bladder of the patient.
  • the implantable element for actively emptying the urinary bladder of the patient is configured to empty the bladder of the patient by compressing the urinary bladder from the outside thereof.
  • the implantable element configured to exert a force on a body portion of the patient is an implantable element for actively stretching a stomach wall of the patient to create a feeling of satiety.
  • a method of implanting an remote unit comprising: placing a second portion of an remote unit between a peritoneum and a layer of muscular tissue of the abdominal wall, placing a first portion of the remote unit between the skin of the patient and a layer of muscular tissue of the abdominal wall, wherein the first and second portions are configured to be connected by a connecting portion extending through at least one layer of muscular tissue of the abdominal wall, placing a body engaging portion of the remote unit in connection with a tissue or an organ of the patient which is to be affected by the remote unit, and placing a transferring member, configured to transfer at least one of energy and force from the second portion to the body engaging portion, at least partially between a peritoneum and a layer of muscular tissue of the abdominal wall, such that at least 1/3 of the length of the transferring member is placed on the outside of the peritoneum.
  • the transferring member is configured to transfer mechanical force from the second portion to the body engaging portion.
  • the transferring member is configured to transfer hydraulic force from the second portion to the body engaging portion.
  • the transferring member is configured to transfer electrical energy force from the second portion to the body engaging portion.
  • the transferring member is configured to transfer data between the second portion and the body engaging portion.
  • the step of placing the transferring member comprises placing the transferring member at least partially between the peritoneum and the layer of muscular tissue of the abdominal wall, such that at least 1/2 of the length of the transferring member is placed on the outside of the peritoneum of the patient.
  • the step of placing the transferring member comprises placing the transferring member at least partially between the peritoneum and the layer of muscular tissue of the abdominal wall, such that at least 2/3 of the length of the transferring member is placed on the outside of the peritoneum of the patient.
  • the step of placing the transferring member comprises placing the transferring member entirely outside of the peritoneum of the patient.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to an area between the rib cage and the peritoneum of the patient, outside of the peritoneum.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to an area between the stomach and the thoracic diaphragm of the patient.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the stomach of the patient.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the esophagus of the patient.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the retroperitoneal space.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to an area of the kidneys.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the renal arteries.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the subperitoneal space, outside of the peritoneum.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the urinary bladder, outside of the peritoneum.
  • the step of placing the transferring member comprises placing the transferring member such that it extends from the second portion to the urethra, outside of the peritoneum.
  • the step of placing the second portion of the remote unit between the peritoneum and the layer of muscular tissue of the abdominal wall comprises placing the second portion between a first and second layer of muscular tissue of the abdominal wall.
  • the step of placing the second portion comprises placing a second portion comprising an electrical motor.
  • the step of placing the second portion comprises placing a second portion comprising a hydraulic pump.
  • the step of placing the second portion comprises placing a second portion comprising an energy storage unit.
  • the step of placing the second portion comprises placing a second portion comprising a receiver for receiving at least one of: energy and communication, wirelessly.
  • the step of placing the first portion comprises placing a first portion comprising a transmitter for transmitting at least one of: energy and communication, wirelessly.
  • the step of placing the second portion comprises placing a second portion comprising a controller involved in the control of the powered medical device.
  • the second portion is elongated and has a length axis extending substantially in the direction of the elongation of the second portion, and wherein the step of placing the second portion comprises placing the second portion such that the length axis is substantially parallel with the cranial -caudal axis of the patient.
  • the second portion is elongated and has a length axis extending substantially in the direction of the elongation of the second portion, and wherein the step of placing the second portion comprises placing the second portion such that the length axis is substantially perpendicular with the cranial -caudal axis of the patient.
  • the second portion is elongated and has a length axis extending substantially in the direction of the elongation of the second portion, and wherein the step of placing the second portion comprises entering a hole in a layer of muscular tissue of the stomach wall in the direction of the length axis of the second portion and pivoting or angling the second portion after the hole has been entered.
  • the step of placing the first portion of the remote unit between the skin of the patient and a layer of muscular tissue of the abdominal wall comprises placing the first portion in the subcutaneous tissue.
  • the step of placing the first portion of the remote unit between the skin of the patient and a layer of muscular tissue of the abdominal wall comprises placing the first portion between a first and second layer of muscular tissue of the abdominal wall.
  • the step of placing the first portion comprises placing a first portion comprising an energy storage unit.
  • the step of placing the first portion comprises placing a first portion comprising a receiver for receiving at least one of: energy and communication, wirelessly.
  • the step of placing the first portion comprises placing a first portion comprising a transmitter for transmitting at least one of: energy and communication, wirelessly.
  • the step of placing the first portion comprises placing a first portion comprising a controller involved in the control of the powered medical device.
  • the first portion is elongated and has a length axis extending substantially in the direction of the elongation of the first portion, and wherein the step of placing the first portion comprises placing the first portion such that the length axis is substantially parallel with the cranial -caudal axis of the patient.
  • the first portion is elongated and has a length axis extending substantially in the direction of the elongation of the first portion, and wherein the step of placing the first portion comprises placing the first portion such that the length axis is substantially perpendicular with the cranial -caudal axis of the patient.
  • the first portion is elongated and has a first portion length axis extending substantially in the direction of the elongation of the first portion
  • the second portion is elongated and has a second portion length axis extending substantially in the direction of the elongation of the second portion
  • the step of placing the first and second portions comprises placing the first and second portions such that the first portion length axis and the second portion length axis are placed at an angle in relation to each other exceeding 30°.
  • the step of placing the first and second portions comprises placing the first and second portions such that the first portion length axis and the second portion length axis are placed at an angle in relation to each other exceeding 45°.
  • the method further comprises the step of placing the connecting portion through at least one layer of muscular tissue of the abdominal wall.
  • the first portion, the second portion and the connecting portion are portions of a single unit.
  • the method further comprises the step of connecting the first portion to the connecting portion, in situ.
  • the method further comprises the step of connecting the second portion to the connecting portion, in situ.
  • the method further comprises the step of connecting the transferring member to the first portion.
  • the method further comprises the step of connecting the transferring member to the body engaging portion.
  • the body engaging portion comprises a medical device for stretching the stomach wall such that a sensation of satiety is created.
  • the body engaging portion comprises a constriction device configured to constrict a luminary organ of a patient.
  • the body engaging portion comprises an implantable constriction device.
  • the implantable constriction device comprises an implantable constriction device for constricting a luminary organ of the patient.
  • the implantable constriction device comprises an implantable constriction device for constricting an intestine of the patient.
  • the implantable constriction device comprises an implantable constriction device for constricting a colon or rectum of the patient.
  • the implantable constriction device comprises an implantable constriction device for constricting the intestine at a region of a stoma of the patient.
  • the implantable constriction device comprises an implantable constriction device for constricting a blood vessel of the patient.
  • the implantable constriction device for constricting a blood vessel of the patient is configured to constrict the venous blood flow leading from an erectile tissue for promoting the engorgement of the erectile tissue.
  • the implantable constriction device for constricting a blood vessel of the patient is configured to constrict the blood flow in the renal artery to affect the patients systemic blood pressure.
  • the implantable constriction device comprises an implantable constriction device for constricting a vas deference of the patient.
  • the body engaging portion comprises an implantable element for actively emptying the urinary bladder of the patient.
  • the implantable element for actively emptying the urinary bladder of the patient is configured to empty the bladder of the patient by compressing the urinary bladder from the outside thereof.
  • the body engaging comprises an element for electrically stimulating a tissue portion of a patient.
  • kits for assembling an remote unit configured to be held in position by a tissue portion of a patient, the kit comprising: a group of one or more first portions, a group of one or more second portions, a group of one or more connecting portions, wherein at least one of said groups comprises at least two different types of said respective portions; wherein the remote unit is a modular device and, when assembled, comprises a selection, from said groups, of one first portion, one second portion, and one connecting portion, wherein: the first portion is configured to be placed on a first side of the tissue portion, the first portion having a first cross-sectional area in a first plane and comprising a first surface configured to face a first tissue surface of the first side of the tissue portion, the second portion is configured to be placed on a second side of the tissue portion, the second side opposing the first side, the second portion having a second cross-sectional area in a second plane and compris
  • the group of one or more first portions comprises a first portion comprising a first energy storage unit.
  • the group of one or more first portions comprises a first portion comprising a first wireless energy receiver unit for receiving energy transmitted wirelessly by an external wireless energy transmitter.
  • the first energy storage unit is connected to the first wireless energy receiver, wherein the first wireless energy receiver is configured to receive energy transmitted wirelessly by the external wireless energy transmitter and store the received energy in the first energy storage unit.
  • the first wireless energy receiver is configured to be physically connected to a second energy storage unit in the second portion.
  • the group of one or more first portions comprises a first portion comprising an internal wireless energy transmitter.
  • the group of one or more second portions comprises a second portion comprising a second wireless energy receiver configured to receive energy transmitted wirelessly by the internal wireless energy transmitter.
  • the internal wireless energy transmitter is configured to transmit energy wirelessly to the second wireless energy receiver.
  • the group of one or more second portions comprises a second portion comprising a second energy storage unit connected to the second wireless energy receiver.
  • the second wireless energy receiver is configured to receive energy transmitted wirelessly by the internal wireless energy transmitter and store the received energy in the second energy storage unit.
  • the group of one or more first portions comprises a first portion being formed as one integral unit with a connecting portion.
  • the group of one or more second portions comprises a second portion being formed as one integral unit with a connecting portion.
  • one of the group of one or more first, second or connecting portions comprises a first portion, second portion and connecting portion being formed as one integral unit.
  • the group of one or more first portions comprises a first portion having a first height along a direction being perpendicular to the first plane, and a first portion having a second height along said direction being perpendicular to the first plane, wherein the second height is larger than the first height.
  • the group of one or more first portions comprises a first portion having a first width and/or length along a direction being parallel to the first plane, and a first portion having a second width and/or length along said direction being parallel to the first plane, wherein the second width and/or length is larger than the first width and/or length.
  • the group of one or more second portions comprises a second portion having a first height along a direction being perpendicular to the second plane, and a second portion having a second height along said direction being perpendicular to the second plane, wherein the second height is larger than the first height.
  • the group of one or more second portions comprises a second portion having a first width and/or length along a direction being parallel to the second plane, and a second portion having a second width and/or length along said direction being parallel to the second plane, wherein the second width and/or length is larger than the first width and/or length.
  • the group of one or more connecting portions comprises a connecting portion having a first height along a direction being perpendicular to the third plane, and a connecting portion having a second height along said direction being perpendicular to the third plane, wherein the second height is larger than the first height.
  • the group of one or more connecting portions comprises a connecting portion having a first width and/or length along a direction being parallel to the third plane, and a connecting portion having a second width and/or length along said direction being parallel to the third plane, wherein the second width and/or length is larger than the first width and/or length.
  • the group of one or more first portions comprises a first portion comprising an injection port for injecting fluid into the first portion.
  • the group of one or more connecting portions comprises a connecting portion comprising a hydraulic fluid conduit for hydraulically connecting the first portion to the second portion.
  • the group of one or more first portions comprises a first portion comprising a first controller comprising at least one processing unit.
  • the group of one or more second portions comprises a second portion comprising a second controller comprising at least one processing unit.
  • At least one of the first and second controller is connected to a wireless transceiver for communicating wirelessly with an external device.
  • the first controller is connected to a first wireless communication receiver in the first portion for receiving wireless communication from an external device, the first controller is connected to a first wireless communication transmitter in the first portion for transmitting wireless communication to a second wireless communication receiver in the second portion.
  • the second controller is connected to the second wireless communication receiver for receiving wireless communication from the first portion.
  • the first wireless energy receiver comprises a first coil and the internal wireless energy transmitter comprises a second coil.
  • the group of first portions comprises a first portion comprising a combined coil, wherein the combined coil is configured to receive wireless energy wirelessly from an external wireless energy transmitter, and transmit wireless energy wirelessly to the second wireless receiver of the second portion.
  • At least one of the coils are embedded in a ceramic material.
  • the group of one or more first portions comprises a first portion comprising a push button and/or a capacitive button for controlling a function of the remote unit.
  • body tissue referred to in the present disclosure may be one or several body tissue groups or layers in a patient, such as muscle tissue, connective tissue, bone, etc.
  • An external device configured for communication with an implantable medical device, when implanted in a patient, is provided.
  • the external device comprises at least one first wireless transceiver configured for communication with the implantable medical device using a first network protocol, for determining a distance between the external device and the implantable medical device, and at least one second wireless transceiver configured for communication with the implantable medical device using a second network protocol, for transferring data between the external device and the implantable medical device.
  • the first wireless transceiver comprises an UWB transceiver.
  • the first wireless transceiver is configured for transcutaneous energy transfer for at least one of powering an energy consuming component of the implantable medical device and charging an implantable energy storage unit.
  • the second network protocol is a standard network protocol.
  • the standard network protocol may be one from the list of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the second wireless transceiver comprises a Bluetooth transceiver.
  • the external device is further configured to communicate with a second external device using said at least one wireless transceiver.
  • the external device is configured for determining a distance between the external device and the implantable medical device by determining the RS SI.
  • a communication range of the first network protocol is less than a communication range of the second network protocol.
  • a frequency band of the first network protocol differs from a frequency band of the second network protocol.
  • the external device is configured to authenticate the implantable medical device if the determined distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the external device is configured to allow the transfer of data between the external device and the implantable medical device after the implantable medical device has been authenticated.
  • the external device is one from the list of: a wearable external device, and a handset.
  • An implantable medical device configured for communication with an external device.
  • the implantable medical device comprises at least one first wireless transceiver configured for communication with the external device using a first network protocol, for determining a distance between the external device and the implantable medical device, and at least one second wireless transceiver configured for communication with the external device using a second network protocol, for transferring data between the external device and the implantable medical device.
  • the first wireless transceiver comprises an UWB transceiver.
  • the first wireless transceiver is configured for transcutaneous energy transfer for at least one of: powering an energy consuming component of the implantable medical device, and charging an implantable energy storage unit.
  • the second network protocol is a standard network protocol, such as selected from the list of Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the second wireless transceiver comprises a Bluetooth transceiver.
  • the implantable medical device is further configured to communicate with a second external device using said at least one wireless transceiver.
  • the implantable medical device is configured for determining a distance between the external device and the implantable medical device by determining the RSSI.
  • a communication range of the first network protocol is less than a communication range of the second network protocol.
  • a frequency band of the first network protocol differs from a frequency band of the second network protocol.
  • the implantable medical device is configured to authenticate the external device if the determined distance between the external device and the implantable medical device is less than a predetermined threshold value.
  • the implantable medical device is configured to allow the transfer of data between the implantable medical device and the external device after the external device has been authenticated.
  • the implantable medical device comprises at least one of: [000810] an external heart compression device,
  • an apparatus assisting the pump function comprising a turbine bump placed within a patient’s blood vessel for assisting the pump function of the heart, [000813] an operable artificial heart valve,
  • an implantable drug delivery device for injecting directly into a blood vessel and change the position of the injection site, all from within the patient’s body
  • an implantable drug delivery device for injecting potency enhancing drugs into an erectile tissue of the patient
  • an implant configured to sense the frequency of the patient ingesting food
  • an operable cosmetic implant for adjust the shape and/or size in the breast region of a patient
  • an implant for affecting the blood flow to an erectile tissue of the patient [000832] an implant for affecting the blood flow to an erectile tissue of the patient, [000833] an implant for simulating the engorgement of an erectile tissue,
  • an implant with a reservoir for holding bodily fluids
  • an implant able to be programmed from outside the body with a wireless signal
  • an implant configured to sense a parameter related to the patient swallowing
  • an implant configured to exercise a muscle with electrical or mechanical stimulation
  • an operable implant configured to be invaginated in the stomach of the patient to reduce the volume of the stomach substantially more than the volume of the device
  • an implant configured for emptying the urinary bladder from within the patient’s body by compressing the bladder
  • an implant configured for draining fluid from within the patient’s body
  • an implant configured for the active lubrication of a joint with an added lubrication fluid
  • an implant configured for removing clots and particles from the patient’s blood stream
  • an implant configured for elongating or straightening a bone in the patient, to reduce scoliosis
  • an artificial stomach replacing the function of the natural stomach
  • an implant configured for adjusting the position of a female’s urinary tract or bladder neck
  • an implant configured for stimulating the ampulla vas deference and creating temporary constriction.
  • the system comprises a master private key device configured to allow issuance of a new private key device, wherein the HCP or HCP admin have such master private key device adapted to able to replace and pair a new patient private key device or HCP private key device into the system, through the HCP EID external device.
  • the patient remote external device and the patient EID external device are an integrated unit.
  • the HCP dedicated device and the HCP EID external device are an integrated unit.
  • the system comprises a measurement device or sensor adapted to deliver a measurement to at least one of the DDI, patent EID external device and a patient display device.
  • the system comprises a food sensor, adapted to measure at least if the patient swallows solid food or is drinking fluid, wherein said food sensor is connected to the control unit of a medical device to cause an action to stretch the stomach after a determined amount of food intake.
  • a patient external device configured for communication with an implantable medical device, when implanted in a patient, is provided.
  • the patient external device comprises a wireless communication unit configured for wireless transmission of control commands to the implantable medical device and configured for wireless communication with a patient display device, and a computing unit configured for running a control software for creating the control commands for the operation of the implantable medical device.
  • the computing unit is configured to transmit a control interface as a remote display portal to a patient display device configured to display the control interface to a user, receive user input from the patient display device, and transform the user input into the control commands for wireless transmission to the implantable medical device.
  • the wireless communication unit comprises a wireless transceiver for wireless transmission of control commands to the implantable medical device, and wireless transmission of the control interface as the remote display portal to the patient display device.
  • the wireless communication unit comprises a first wireless transceiver for wireless transmission of control commands to the implantable medical device, and a second wireless transceiver for wireless transmission of the control interface to the patient display device.
  • the wireless communication unit is configured for wireless communication with the patient display device using a standard network protocol.
  • the wireless communication unit is configured for wireless communication with the implantable medical device using a proprietary network protocol.
  • the wireless communication unit comprises a Bluetooth transceiver.
  • At least one of the first and second wireless transceiver comprises a Bluetooth transceiver.
  • the wireless communication unit comprises a UWB transceiver.
  • At least one of the first and second wireless transceiver comprises a UWB transceiver.
  • the wireless communication unit comprises at least one first wireless transceiver configured for communication with the implantable medical device using a first network protocol, for determining a distance between the patient external device and the implantable medical device, and at least one second wireless transceiver configured for communication with the implantable medical device using a second network protocol, for transferring data between the patient external device and the implantable medical device.
  • the first wireless transceiver is configured for transcutaneous energy transfer for at least one of: powering an energy consuming component of the implantable medical device and charging an implantable energy storage unit.
  • the standard network protocol is one from the list of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • a communication range of the first wireless transceiver is less than a communication range of the second wireless transceiver.
  • the patient external device is configured to authenticate the implantable medical device if a distance between the patient external device and the implantable medical device is less than a predetermined threshold value
  • the patient external device is configured to be authenticated by the implantable medical device if a distance between the patient external device and the implantable medical device is less than a predetermined threshold value
  • the patient external device is configured to authenticate the patient display device if a distance between the patient external device and the patient display device is less than a predetermined threshold value
  • the patient external device is configured to be authenticated by the implantable medical device if a distance between the patient external device and the patient display device is less than a predetermined threshold value.
  • the patient external device is configured to allow the transfer of data between at least one of: the patient external device and the implantable medical device, and the patient external device and the patient display device, on the basis of the authentication.
  • the computing unit is configured to encrypt at least one of the control interface and the control commands.
  • the implantable medical device comprises at least one of: [000897] an external heart compression device,
  • an apparatus assisting the pump function comprising a turbine bump placed within a patient’s blood vessel for assisting the pump function of the heart
  • an operable artificial heart valve for increasing the blood flow to the coronary arteries.
  • an implantable drug delivery device for injecting directly into a blood vessel and change the position of the injection site, all from within the patient’s body
  • an implantable drug delivery device for injecting potency enhancing drugs into an erectile tissue of the patient
  • an implant configured to sense the frequency of the patient ingesting food
  • an operable cosmetic implant for adjust the shape and/or size in the breast region of a patient
  • an implant with a reservoir for holding bodily fluids
  • an implant storing and/or emptying a bodily reservoir or a surgically created
  • an implant configured to sense a parameter related to the patient swallowing
  • an implant configured to exercise a muscle with electrical or mechanical stimulation
  • an operable implant configured to be invaginated in the stomach of the patient to reduce the volume of the stomach substantially more than the volume of the device
  • an implant configured for emptying the urinary bladder from within the patient’s body by compressing the bladder
  • an implant configured for draining fluid from within the patient’s body
  • an implant configured for the active lubrication of a joint with an added lubrication fluid
  • an implant configured for removing clots and particles from the patient’s blood stream
  • an implant configured for elongating or straightening a bone in the patient, to reduce scoliosis
  • an implant configured for adjusting the position of a female’s urinary tract or bladder neck
  • an implant configured for stimulating the ampulla vas deference and creating temporary constriction.
  • the system comprises a master private key device configured to allow issuance of a new private key device, wherein the HCP or HCP admin have such master private key device adapted to able to replace and pair a new patient private key device or HCP private key device into the system, through the HCP EID external device.
  • the patient remote external device and the patient EID external device are an integrated unit.
  • the HCP dedicated device and the HCP EID external device are an integrated unit.
  • the system comprises a measurement device or sensor adapted to deliver a measurement to at least one of the DDI, patent EID external device and a patient display device.
  • the system comprises a food sensor, adapted to measure at least if the patient swallows solid food or is drinking fluid, wherein said food sensor is connected to the control unit of a medical device to cause an action to stretch the stomach after a determined amount of food intake.
  • a patient display device for communication with a patient remote external device for communication with an implantable medical device.
  • the patient display device comprises a wireless communication unit configured for wirelessly receiving an implant control interface as a remote display portal from the patient remote external device and configured for wirelessly transmitting implant control user input to the patient remote external device, a display for displaying the received implant control interface, and an input device for receiving implant control input from the user.
  • the patient display device further comprises an auxiliary wireless communication unit.
  • the auxiliary wireless communication unit is configured to be disabled to enable at least one of: wirelessly receiving the implant control interface as the remote display portal from the patient remote external device, and wirelessly transmitting implant control user input to the patient remote external device.
  • the wireless communication unit is configured for wireless communication with the patient remote external device using a standard network protocol.
  • the standard network protocol may be one from the list of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • the wireless communication unit is configured for wireless communication with the patient remote external device using a proprietary network protocol.
  • the wireless communication unit comprises a Bluetooth transceiver.
  • the wireless communication unit comprises a UWB transceiver.
  • a communication range of the wireless communication unit is less than a communication range of the auxiliary wireless communication unit.
  • the patient display device is configured to authenticate the patient remote external device if a distance between the patient display device and the patient remote external device is less than a predetermined threshold value, or to be authenticated by the patient remote external device if a distance between the patient display device and the patient remote external device is less than a predetermined threshold value.
  • the patient display device is configured to allow the transfer of data between the patient display device and the patient remote external device on the basis of the authentication.
  • the patient display device is a wearable external device or a handset.
  • the system comprises a master private key device configured to allow issuance of a new private key device, wherein the HCP or HCP admin have such master private key device adapted to able to replace and pair a new patient private key device or HCP private key device into the system, through the HCP EID external device.
  • the patient remote external device and the patient EID external device are an integrated unit.
  • the HCP dedicated device and the HCP EID external device are an integrated unit.
  • the system comprises a measurement device or sensor adapted to deliver a measurement to at least one of the DDI, patent EID external device and a patient display device.
  • the system comprises a food sensor, adapted to measure at least if the patient swallows solid food or is drinking fluid, wherein said food sensor is connected to the control unit of a medical device to cause an action to stretch the stomach after a determined amount of food intake.
  • a communication system for enabling communication between a patient display device and an implantable medical device, when implanted, comprises: a patient display device, [000978] a server, and a patient remote external device.
  • the patient display device comprises a wireless communication unit configured for wirelessly receiving an implant control interface as a remote display portal being provided by the patient remote external device.
  • the wireless communication unit is further configured for wirelessly transmitting implant control user input to the server, destined for the patient remote external device.
  • the system further comprises a display for displaying the received remote display portal, and an input device for receiving implant control input from the user, wherein the patient remote external device comprises a wireless communication unit configured for wireless transmission of control commands to the implantable medical device, and a computing unit.
  • the computing unit is configured for running a control software for creating the control commands for the operation of the implantable medical device, transmitting a control interface to the patient display device, receiving implant control user input generated at the patient display device, from the server, and transforming the user input into the control commands for wireless transmission to the implantable medical device.
  • the computing unit is configured to encrypt at least one of the control interface and the control commands.
  • the patient display device is configured to encrypt the user input.
  • the server is configured to encrypt at least one of the user input received from the patient display device and the control interface received from the patient remote external device.
  • the computing unit is configured to encrypt the control interface and the patient display device is configured to decrypt the encrypted control interface.
  • the server is configured to act as a router, transferring the encrypted control interface from the patient remote external device to the patient display device without decryption.
  • the implantable medical device comprises at least one of:
  • an apparatus assisting the pump function comprising a turbine bump placed within a patient’s blood vessel for assisting the pump function of the heart,
  • an operable artificial heart valve for increasing the blood flow to the coronary arteries.
  • an implantable drug delivery device for injecting directly into a blood vessel and change the position of the injection site, all from within the patient’s body
  • an implantable drug delivery device for injecting potency enhancing drugs into an erectile tissue of the patient
  • an implant configured to sense the frequency of the patient ingesting food
  • an operable cosmetic implant for adjust the shape and/or size in the breast region of a patient
  • an implant storing and/or emptying a bodily reservoir or a surgically created
  • an implant for hindering the transportation of the sperm in the vas deferens [0001020] an implant treating osteoarthritis,
  • an implant controlling the blood pressure by affecting the dilatation of the renal artery [0001026] an implant controlling a drug treatment parameter, [0001027] an implant controlling a parameter in the blood,
  • an implant configured to sense a parameter related to the patient swallowing
  • an implant configured to exercise a muscle with electrical or mechanical stimulation
  • an operable implant configured to be invaginated in the stomach of the patient to reduce the volume of the stomach substantially more than the volume of the device
  • an implant configured for emptying the urinary bladder from within the patient’s body by compressing the bladder
  • an implant configured for draining fluid from within the patient’s body
  • an implant configured for the active lubrication of a joint with an added lubrication fluid
  • an implant configured for removing clots and particles from the patient’s blood stream
  • an implant configured for elongating or straightening a bone in the patient, to reduce scoliosis
  • a device to stimulate the brain for a several position to a focused point [0001042] an artificial stomach replacing the function of the natural stomach, [0001043] an implant configured for adjusting the position of a female’s urinary tract or bladder neck,
  • an implant configured for stimulating the ampulla vas deference and creating temporary constriction.
  • the communication system further comprises a server.
  • the server may comprise a wireless communication unit configured for wirelessly receiving an implant control interface received from the patient remote external device and wirelessly transmitting the implant control interface as a remote display portal to the patient display device.
  • the wireless communication unit is further configured for wirelessly receiving implant control user input from a patient EID external device and wirelessly transmitting the implant control user input to the patient display device.
  • the system comprises a master private key device configured to allow issuance of a new private key device, wherein the HCP or HCP admin have such master private key device adapted to able to replace and pair a new patient private key device or HCP private key device into the system, through the HCP EID external device.
  • the patient remote external device and the patient EID external device are an integrated unit.
  • the HCP dedicated device and the HCP EID external device are an integrated unit.
  • the system comprises a measurement device or sensor adapted to deliver a measurement to at least one of the DDI, patent EID external device and a patient display device.
  • the system comprises a food sensor, adapted to measure at least if the patient swallows solid food or is drinking fluid, wherein said food sensor is connected to the control unit of a medical device to cause an action to stretch the stomach after a determined amount of food intake.
  • a patient display device for communication with a patient external device for communication with an implantable medical device, when implanted, is provided.
  • the patient display device comprises a wireless communication unit, a display, and an input device for receiving implant control input from the user.
  • the patient display device is configured to run a first application for wireless communication with a server and/or DDI, and run a second application for wireless communication with the patient external device for transmission of the implant control input to a remote display portal of the patient external device for the communication with the implantable medical device, wherein the second application is configured to be accessed through the first application.
  • the patient display device comprises a first log-in function and a second log-in function, wherein the first log-in function gives the user access to the first application and wherein the first and second log-in function in combination gives the user access to the second application.
  • the first log-in function may be configured to use at least one of a password, pin code, fingerprint, voice and face recognition.
  • a second log-in function within the first application may be configured to use a private key from the user to authenticate, for a defined time period, a second hardware key of the patient external device.
  • the first log-in is a PIN-based log-in.
  • At least one of the first and second log-in is a log-in based on a biometric input or a hardware key.
  • the patient display device further comprises an auxiliary wireless communication unit, and wherein the auxiliary wireless communication unit is configured to be disabled to enable wireless communication with the patient external device.
  • the patient display device is configured to wirelessly receive an implant control interface as a remote display portal from the patient external device to be displayed on the display.
  • the wireless communication unit is configured for wireless communication with the patient external device using a standard network protocol.
  • the wireless communication unit is configured for wireless communication with the patient external device using a proprietary network protocol.
  • the wireless communication unit is configured for wireless communication with the patient external device using a first network protocol and with the server using a second network protocol.
  • the wireless communication unit is configured for wireless communication with the patient external device using a first frequency band and with the server using a second frequency band.
  • the wireless communication unit comprises a Bluetooth transceiver.
  • the wireless communication unit comprises a UWB transceiver.
  • the standard network protocol is one from the list of: Radio Frequency type protocol, RFID type protocol, WLAN type protocol, Bluetooth type protocol, BLE type protocol, NFC type protocol, 3G/4G/5G type protocol, and GSM type protocol.
  • a communication range of the wireless communication unit is less than a communication range of the auxiliary wireless communication unit.
  • the wireless communication unit comprises a first wireless transceiver for communication with the patient external device and a second wireless transceiver for communication with the server.
  • the second wireless transceiver is configured to be disabled to enable wireless communication using the first wireless transceiver.
  • the patient display device is configured to authenticate the patient external device if a distance between the patient display device and the patient external device is less than a predetermined threshold value, or to be authenticated by the patient external device if a distance between the patient display device and the patient external device is less than a predetermined threshold value.
  • the patient display device is configured to allow the transfer of data between the patient display device and the patient external device on the basis of the authentication.
  • the patient display device is a wearable external device or a handset.
  • the second application is configured to receive data related to a parameter of the implanted medical device.
  • the second application is configured to receive data related to a sensor value received from the implanted medical device.
  • the second application is configured to receive data related to a parameter related to at least one of: a battery status, a temperature, a time, and an error.
  • the patient display device is configured to encrypt the user input.
  • the display is configured to encrypt the user input for decryption by the implantable medical device.
  • the patient display device is configured to decrypt the control interface received from the patient external device, for displaying the control interface on the display.
  • At least one of the first and second application is configured to receive data from an auxiliary external device and present the received data to the user.
  • at least one of the first and second application is configured to receive data from an auxiliary external device comprising a scale for determining the weight of the user.
  • At least one of the first and second application is configured to receive data related to the weight of the user from an auxiliary external device comprising a scale.
  • the patient display device is configured to: wirelessly transmit the data related to the weight of the user to the patient external device, or wirelessly transmit an instruction derived from the data related to the weight of the user, or wirelessly transmit an instruction derived from a combination of the data related to the weight of the user and the implant control input received from the user.
  • the system comprises a master private key device configured to allow issuance of a new private key device, wherein the HCP or HCP admin have such master private key device adapted to able to replace and pair a new patient private key device or HCP private key device into the system, through the HCP EID external device.
  • the patient remote external device and the patient EID external device are an integrated unit.
  • the HCP dedicated device and the HCP EID external device are an integrated unit.
  • the system comprises a measurement device or sensor adapted to deliver a measurement to at least one of the DDI, patent EID external device and a patient display device.
  • the system comprises a food sensor, adapted to measure at least if the patient swallows solid food or is drinking fluid, wherein said food sensor is connected to the control unit of a medical device to cause an action to stretch the stomach after a determined amount of food intake.
  • a communication system for enabling communication between a patient display device and an implantable medical device, when implanted, is provided.
  • the communication system comprises a patient display device,
  • the patient display device comprises a wireless communication unit configured for wirelessly receiving an implant control interface as a remote display portal from the patient remote external device, the wireless communication unit further being configured for wirelessly transmitting implant control user input to the patient remote external device, a display for displaying the received implant control interface as a remote display portal, and an input device for receiving implant control input from the user.
  • the patient display device is configured to run a first application for wireless communication with the server, and to run a second application for wireless communication with the patient remote external device for transmission of the implant control input to the remote display portal of the patient remote external device for the communication with the implantable medical device.
  • the patient remote external device comprises a wireless communication unit configured for wireless transmission of control commands based on the implant control input to the implantable medical device and configured for wireless communication with the patient display device.
  • the patient display device comprises a first log-in function and a second log-in function, and wherein the first log-in function gives the user access to the first application and wherein the first and second log-in function in combination gives the user access to the second application.
  • the second application is configured to receive data related to a parameter of the implanted medical device.
  • the second application is configured to receive data related to a sensor value received from the implanted medical device.
  • the second application is configured to receive data related to a parameter related to at least one of: a battery status, [0001091] a temperature, a time, or an error.
  • the patient display device is configured to encrypt the user input.
  • the display is configured to encrypt the user input for decryption by the implantable medical device.
  • the patient remote external device is configured to act as a router, transferring the encrypted user input from the patient display device to the implantable medical device without decryption.
  • the patient remote external device is configured to encrypt at least one of the control interface and the control commands.
  • the patient remote external device is configured to encrypt the control interface and wherein the patient display device is configured to decrypt the encrypted control interface.
  • a computer program product configured to run in a patient display device comprising a wireless communication unit, a display for displaying the received implant control interface as a remote display portal, and an input device for receiving implant control input from a user.
  • the computer program product comprises:
  • a second application for communication with an patient remote external device for transmission of the implant control input via the remote display portal of the patient remote external device for the communication with an implantable medical device, wherein the second application is configured to be accessed through the first application,
  • a first log-in function using at least one of a password, pincode, fingerprint, or face recognition
  • a second log-in function within the first application using a private key from the user to authenticate for a defined time period a second hardware key of the patient remote external device.
  • the first log-in function gives the user access to the first application and the first and second log-in function in combination gives the user access to the second application.
  • the second application is configured to receive data related to a parameter of the implanted medical device.
  • the second application is configured to receive data related to a sensor value received from the implanted medical device.
  • the second application is configured to receive data related to a parameter related to at least one of: a battery status, [0001105] a temperature, a time, or an error.
  • the implantable medical device comprises at least one of:
  • an apparatus assisting the pump function comprising a turbine bump placed within a patient’s blood vessel for assisting the pump function of the heart,
  • an implantable drug delivery device for injecting directly into a blood vessel and change the position of the injection site, all from within the patient’s body
  • an implantable drug delivery device for injecting potency enhancing drugs into an erectile tissue of the patient

Abstract

L'invention concerne un dispositif médical pour étirer activement une paroi gastrique d'un patient afin de créer une sensation de satiété. Le dispositif médical est implantable et comprend un premier élément conçu pour être fixé à une première partie de la paroi gastrique, un second élément conçu pour être fixé à une seconde partie de la paroi gastrique, un dispositif d'actionnement pour faire fonctionner le second élément afin de déplacer le second élément dans une première direction par rapport au premier élément, en vue d'étirer la paroi gastrique entre les première et seconde parties.
PCT/EP2023/053903 2022-02-18 2023-02-16 Dispositif d'étirage WO2023156529A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
SE2250181 2022-02-18
SE2250181-1 2022-02-18
EPPCT/EP2022/073784 2022-08-26
PCT/EP2022/073784 WO2023031038A1 (fr) 2021-08-30 2022-08-26 Dispositif d'étirage

Publications (1)

Publication Number Publication Date
WO2023156529A1 true WO2023156529A1 (fr) 2023-08-24

Family

ID=85227023

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2023/053903 WO2023156529A1 (fr) 2022-02-18 2023-02-16 Dispositif d'étirage

Country Status (1)

Country Link
WO (1) WO2023156529A1 (fr)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2015205843A1 (en) * 2008-01-29 2015-08-13 Implantica Patent Ltd. A device, system and method for treating obesity
EP3049034A1 (fr) * 2013-09-29 2016-08-03 Institut Hospitalo-Universitaire de Chirurgie Mini -Invasive Guidee Par l'Image Dispositif iimplantable pour traiter l'obésité
US20200253769A1 (en) * 2015-03-17 2020-08-13 Appetec, Inc. Systems and Methods for Weight Management including Virtual Reality, Artificial Intelligence, Accountability Integration, and Biofeedback

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2015205843A1 (en) * 2008-01-29 2015-08-13 Implantica Patent Ltd. A device, system and method for treating obesity
EP3049034A1 (fr) * 2013-09-29 2016-08-03 Institut Hospitalo-Universitaire de Chirurgie Mini -Invasive Guidee Par l'Image Dispositif iimplantable pour traiter l'obésité
US20200253769A1 (en) * 2015-03-17 2020-08-13 Appetec, Inc. Systems and Methods for Weight Management including Virtual Reality, Artificial Intelligence, Accountability Integration, and Biofeedback

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