Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M25/00—Catheters; Hollow probes
  • A61M25/0043—Catheters; Hollow probes characterised by structural features
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M25/00—Catheters; Hollow probes
  • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
  • A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
  • A61M25/0113—Mechanical advancing means, e.g. catheter dispensers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150015—Source of blood
  • A61B5/15003—Source of blood for venous or arterial blood
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150206—Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150206—Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
  • A61B5/150259—Improved gripping, e.g. with high friction pattern or projections on the housing surface or an ergonometric shape
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
  • A61B5/150534—Design of protective means for piercing elements for preventing accidental needle sticks, e.g. shields, caps, protectors, axially extensible sleeves, pivotable protective sleeves
  • A61B5/150633—Protective sleeves which are axially extensible, e.g. sleeves connected to, or integrated in, the piercing or driving device; pivotable protective sleeves
  • A61B5/150641—Protective sleeves which are axially extensible, e.g. sleeves connected to, or integrated in, the piercing or driving device; pivotable protective sleeves comprising means to impede repositioning of protection sleeve from covering to uncovering position
  • A61B5/150656—Protective sleeves which are axially extensible, e.g. sleeves connected to, or integrated in, the piercing or driving device; pivotable protective sleeves comprising means to impede repositioning of protection sleeve from covering to uncovering position semi-automatically triggered, i.e. in which the triggering of the protective sleeve requires a deliberate action by the user, e.g. manual release of spring-biased extension means
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150801—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming
  • A61B5/150809—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming by audible feedback
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150801—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming
  • A61B5/150816—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming by tactile feedback, e.g. vibration
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150007—Details
  • A61B5/150801—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming
  • A61B5/150824—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming by visual feedback
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/150992—Blood sampling from a fluid line external to a patient, such as a catheter line, combined with an infusion line; Blood sampling from indwelling needle sets, e.g. sealable ports, luer couplings or valves
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B5/00—Measuring for diagnostic purposes; Identification of persons
  • A61B5/15—Devices for taking samples of blood
  • A61B5/153—Devices specially adapted for taking samples of venous or arterial blood, e.g. with syringes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M25/00—Catheters; Hollow probes
  • A61M25/0043—Catheters; Hollow probes characterised by structural features
  • A61M2025/0059—Catheters; Hollow probes characterised by structural features having means for preventing the catheter, sheath or lumens from collapsing due to outer forces, e.g. compressing forces, or caused by twisting or kinking

Definitions

• the present disclosure relates generally to medical devices for use with intravenous (IV) catheters and, more specifically, to medical devices with features for limiting deflection of flexible catheters.
• IV intravenous
• Blood collection devices when used with indwelling IV catheters, can include displaceable catheters that are advanced beyond the tip of the indwelling catheter for blood collection. Often, when the displaceable catheter is advanced, it can encounter an obstruction, resulting in deflection of the catheter. Examples of obstructions include the friction of the seal within the blood collection device, torturous path within an integrated catheter, pinching of the catheter tubing as it dives into the skin, thrombus, fibrin, and valves. Such deflections can reduce the ability of the displaceable catheter to extend beyond the tip of the indwelling catheter, and thus limits their use for blood collection. Accordingly, a need exists in the art for devices that limit buckling, and that ensure timely and effective blood collection.
• a medical device including a catheter having a proximal end, a distal end, and a sidewall therebetween defining a lumen therethrough, an introducer having a proximal end, a distal end, and a sidewall therebetween defining an inner volume configured to movably receive the catheter, the distal end of the introducer having a lock configured to couple the introducer to an intravenous line, the introducer further having a flexible member arranged within the inner volume configured to limit deflection of the catheter as the catheter is moved within the introducer, and an actuator movably coupled to the introducer, the actuator having a first portion disposed outside of the introducer and a second portion disposed in the inner volume of the introducer and coupled to the catheter, the actuator configured to move relative to the introducer to move the catheter between a first position, in which the catheter is disposed within the introducer, and a second position, in which the distal end of the catheter is disposed beyond the distal end of the introducer such that
• the flexible member is arranged along a longitudinal axis within the inner volume of the introducer.
• the flexible member may include an elastomeric material.
• the flexible member and the introducer define a substantially cylindrical passage within which the catheter is received.
• the flexible member may extend from the proximal end of the introducer to the distal end.
• the flexible member is a unitary member.
• the flexible member may include a plurality of flexible members.
• the plurality of flexible members may be arranged about a perimeter of the inner volume.
• the plurality of flexible members may substantially surround the catheter.
• the second portion of the actuator displaces the flexible member.
• the second portion of the actuator may be coupled to the proximal end of the catheter.
• a lubricant may be received within the inner volume.
• a medical device including a catheter having a proximal end, a distal end, and a sidewall therebetween defining a lumen therethrough, an introducer having a proximal end, a distal end, and a sidewall therebetween defining an inner volume configured to movably receive the catheter, the distal end of the introducer having a lock configured to couple the introducer to an intravenous line, the introducer further having a flexible member arranged within the inner volume, and an actuator coupled to the catheter, the actuator configured to move relative to the introducer in response to a first force exerted on the actuator to move the catheter between a first position, in which the distal end of the catheter is disposed within the lumen of the lock, and a second position, in which the catheter extends through the lock and intravenous line when the lock is coupled to the intravenous line such that the distal end of the catheter is disposed within the intravenous line, wherein the actuator is configured to exert a second force different from the
• the actuator includes a first portion disposed outside of the introducer and a second portion disposed within the introducer, and the first force exerted on the actuator is exerted on the first portion of the actuator, the second force exerted by the actuator is exerted by the second portion of the actuator.
• the flexible member may be arranged along a longitudinal axis within the inner volume of the introducer.
• the flexible member may include an elastomeric material.
• the flexible member and the introducer may define a substantially cylindrical passage within which the catheter is received.
• the flexible member may extend from the proximal end of the introducer to the distal end.
• the flexible member may be a unitary member.
• the flexible member may include a plurality of flexible members.
• the plurality of flexible members may be arranged about a perimeter of the inner volume. In other configurations, the plurality of flexible members may substantially surround the catheter.
• the second portion of the actuator displaces the flexible member.
• the second portion of the actuator may be coupled to the proximal end of the catheter.
• the device may further include a lubricant received within the inner volume.
• a medical device including a catheter having a proximal end, a distal end, and a sidewall therebetween defining a lumen therethrough, an introducer having a proximal end, a distal end, and a sidewall therebetween defining an inner volume configured to movably receive the catheter, the distal end of the introducer having a lock configured to couple the introducer to an intravenous line, the inner volume configured to limit deflection of the catheter as the catheter is moved within the introducer, an actuator movably coupled to the introducer, the actuator having a first portion disposed outside of the introducer and a second portion disposed in the inner volume of the introducer and coupled to the catheter, the actuator configured to move relative to the introducer to move the catheter between a first position, in which the catheter is disposed within the introducer, and a second position, in which the distal end of the catheter is disposed beyond the distal end of the introducer such that at least a first portion of the catheter is disposed within
• FIG. 1 is a perspective view of a medical device according to non-limiting embodiments described herein;
• FIG. 2 is an exploded perspective view of a medical device according to non-limiting embodiments described herein;
• FIG. 3 is an exploded perspective view of a medical device according to non-limiting embodiments described herein;
• FIG. 4 is an exploded perspective view of a medical device according to non-limiting embodiments described herein;
• FIG. 5 is a cross-sectional view of a prior medical device
• FIG. 6 is a cross-sectional view of a medical device according to non-limiting embodiments described herein;
• FIG. 7 is a cross-sectional view of a medical device according to non-limiting embodiments described herein;
• FIG. 8 is a front view of an actuator for a medical device according to non-limiting embodiments described herein;
• FIG. 9 is a cross-sectional view of a medical device according to non-limiting embodiments described herein;
• FIG. 10 is a cross-sectional view of a medical device according to non-limiting embodiments described herein;
• FIG. 11 is a cross-sectional view of a medical device according to non-limiting embodiments described herein;
• FIG. 12A is a cross-sectional view of a prior medical device.
• FIG. 12B is a cross-sectional view of a medical device according to non-limiting embodiments described herein.
• a range of “1 to 10” is intended to include all sub-ranges between (and including) the recited minimum value of 1 and the recited maximum value of 10, that is, having a minimum value equal to or greater than 1 and a maximum value of equal to or less than 10.
• a medical device with a displaceable medical implement such as a displaceable catheter.
• exemplary medical devices include those utilized for blood collection from indwelling IV catheters, such as peripheral IV catheters, and have displaceable catheters that can be displaced such that a tip of the displaceable catheter extends beyond a tip of the indwelling IV catheter.
• the displaceable catheter can encounter a resistive force, whether in the form of an occlusion at the tip of the indwelling IV catheter, a thrombus within the blood vessel, friction within the medical device, pinching of the catheter as the catheter curves to match the angle at which the IV catheter enters the patient’s skin, or combinations thereof.
• resistive forces can result in deflection (e.g., buckling) of the displaceable catheter.
• devices as described herein include features for limiting deflection of displaceable implements (e.g., catheters) in medical devices.
• FIGS. 1-4 shown is a non-limiting embodiment of a medical device 100. While exemplified as a fluid transfer device, those of skill in the art will appreciate that the deflection-limiting features described herein will be suitable for any medical device with a displaceable implement that is subject to deflection, for example flexible, displaceable components.
• medical device 100 includes an introducer 110 having a distal end 112 and a proximal end 114, with a sidewall 116 therebetween defining an inner volume 118.
• inner volume 118 may include a first portion 118a and a second portion 118b, which may or may not be fluidly isolated from one another.
• Introducer 110 may include, at distal end 112 thereof, a lock 130 and blunt cannula 132, for coupling to an IV catheter (not shown), a catheter adapter (not shown), or the like. Introducer 110 may be any suitable size and/or shape, and may be formed of any suitable material(s), such as plastic(s). While lock 130 is exemplified in the present figures as a plurality of arms and blunt cannula 132, those of skill will appreciate that any connection or coupling, for example a luer, can be used, so long as distal end 152 of catheter 150 may pass through the connection to access a medical device, such as an IV catheter to which introducer 110 is coupled.
• introducer 110 may be formed of two housing portions, a first housing portion 120 and a second housing 122.
• First and second housing portions 120, 122 can be coupled together by any suitable method, for example a snap fit, friction fit, ultrasonic weld, and/or adhesive.
• Combined housing portions 120, 122 may define inner volume 118, and one or more features on interior surfaces of housing portions 120, 122 may define first and second inner volume portions 118a, 118b.
• Medical device 100 may further include one or more catheters.
• medical device 100 includes a catheter 150 and, optionally, a secondary catheter 160.
• Secondary catheter 160 may be used to couple with, for example through coupler 170, a vacuum (air or liquid) source, a blood collection tube, a fluid reservoir, fluid source, syringe, and/or the like, which in turn, may place the catheter 150 in fluid communication therewith.
• coupler 170 e.g., a coupler, such as coupler 170, may be provided on proximal end 114 of introducer 110).
• Catheter 150 may have a distal end 152, proximal end 154, and a sidewall 156 therebetween defining a lumen therethrough.
• Catheter 150 may be of any suitable length and gauge, and may be formed of any suitable material in any suitable configuration (e.g., braiding).
• catheter 150 is from 10-30 gauge, all values and subranges therebetween inclusive.
• catheter 150 may be formed of a relatively flexible biocompatible material with a Shore durometer of about 20 Shore A to 50 Shore D; about 20 Shore A to 95 Shore D; about 70 Shore D to 85 Shore D, and/or any other suitable range of Shore durometer.
• catheter 150 may be formed of a braided material or the like, which can modify, change, and/or alter a flexibility of catheter 150 in response to a bending force or the like.
• catheter 150 is formed of a polyimide-containing material.
• catheter 150 is of a pre-determined length such that, when fully displaced distally, distal end 152 extends beyond a distal end of an IV catheter. In non-limiting embodiments, the predetermined length may be indicated by one or more indicia on introducer 110.
• Secondary catheter 160 may have a distal end 162, proximal end 164, and a sidewall 166 defining a secondary lumen therethrough.
• secondary catheter 160 may include a coupler 170 at proximal end 164 thereof.
• Coupler 170 may be any suitable connection or coupler, for example a luer, a needleless connector, or like connector known to those of skill in the art.
• Secondary catheter 160 may be of any suitable length and gauge, and may be formed of any suitable material in any suitable configuration (e.g., braiding). In non-limiting embodiments, secondary catheter 160 is from 10-30 gauge, all values and subranges therebetween inclusive. In non-limiting embodiments, secondary catheter 160 is a polyimide- containing material.
• secondary catheter 160 is in fluid communication with catheter 150.
• catheter 150 and secondary catheter 160 are configured to place a fluid reservoir, such as a blood collection tube (e.g., an evacuated tube) in fluid communication with the IV catheter, thus allowing for blood to be collected from the IV catheter.
• a fluid reservoir such as a blood collection tube (e.g., an evacuated tube) in fluid communication with the IV catheter, thus allowing for blood to be collected from the IV catheter.
• Medical device 100 may also include an actuator 180, which may be coupled to catheter 150.
• actuator 180 is coupled to proximal end 154 of catheter 150.
• Actuator 180 may be manipulated by a user, such as a medical professional, to transition the device 100 from a first configuration, in which distal end 152 of catheter 150 is proximal of the IV catheter, to a second configuration in which at least distal end 152 of catheter 150 is disposed in a distal position relative to the IV catheter.
• a user such as a medical professional
• FIG. 8 shown is a non-limiting embodiment of actuator 180, in which actuator 180 includes a first portion 181 having an engagement member 182 and tab 183, second portion 185 including opening 186, and wall 187 therebetween.
• Engagement member 182 may be configured to be contacted by a finger of a user.
• Wall 187 may connect first portion 181 and second portion 185.
• inner volume 118 of introducer 110 can have a tortuous cross-sectional shape.
• Wall 187 may be configured to match such a tortuous shape.
• Opening 186 may be included in second portion 185, and may be coupled with catheter 150 at any position along a length thereof. Coupling between catheter 150 and opening 186 may be accomplished through any known means, for example friction fit, ultrasonic weld, adhesives, or combinations thereof.
• Tab 183 may include one or more features that interact with an outer surface of introducer 100, for example, to provide tactile, acoustic, and/or visual feedback.
• Such feedback can inform a user, for example, of how far catheter 150 has been displaced, including whether distal end 152 of catheter 150 is in a distal position relative to the IV catheter.
• a first force is exerted on actuator 180 by a user to move actuator 180 relative to introducer 110 to advance catheter 150 from a first position, in which distal end 152 of catheter 150 is disposed within a lumen defined by lock 130, toward a second position.
• a second force, different from the first force, is exerted by actuator 180, for example by virtue of interaction between second actuator portion 185 and catheter 150, on catheter 150, for example on proximal end 154 of catheter 150, as actuator 180 is advanced, displacing catheter 150 from the first position toward the second position.
• catheter 250 may be deflected if catheter 250 encounters an obstruction during deployment by actuator 280 and/or if there is friction between catheter 250 and any portion of device 200, as described previously. This deflection can increase beyond an acceptable amount, resulting in an inability to move distal end of catheter 250 to the second position (a distal position relative to the IV catheter).
• introducer 110 of medical device 100 may include a flexible member 124 arranged within inner volume 118 to limit deflection of catheter 150. Without wishing to be bound by the theory, it is believed that reducing the volume in which catheter 150 resides allows for an increase in force that can be applied to catheter 150, to bypass occlusions or blockages without an unacceptable level of deflection being exhibited.
• Flexible member 124 may be connected to introducer 110 through a snap fit, friction fit, ultrasonic weld, adhesives, or combinations thereof. Flexible member 124 may be arranged within introducer 110 in any suitable configuration, so long it serves to limit deflection of catheter 150. In non-limiting embodiments, flexible member 124 extends along a substantial (e.g., more than 50%) length of introducer 110. In some embodiments, flexible member 124 extends along the complete length of the inner volume 118 of introducer 110. In some embodiments, flexible member 124 may mark a separation between inner volume first portion 118a and inner volume second portion 118b. Flexible member 124 may be formed of any suitable material.
• flexible member 124 is formed of a material that allows flexible member 124 to maintain sufficient flexibility to allow flexible member 124 to be displaced by actuator 180 (e.g., wall 187) as actuator moves catheter 150 through inner volume 118.
• flexible member 124 is formed of a material with sufficient resiliency such that flexible member 124 returns to its original configuration following transit of actuator 180, thereby maintaining a barrier that limits deflection of catheter 150 within inner volume 118.
• flexible member 124 is shown as being connected to and/or part of first introducer housing portion 120, those of skill in the art will appreciate that flexible member 124 may be connected to one or both housing portions 120, 122, and may assume any orientation/angle relative thereto, so long as flexible member 124 limits deflection of catheter 150.
• flexible member 124 may be oriented in a number of distinct ways in terms of angle and connection to one or more housing portions, and may, in some embodiments, form a border within inner volume 118, providing an inner volume second portion 118b that provides catheter 150 with less space than a total space of inner volume 118 within which deflection can occur.
• medical device 300 may include introducer 310, catheter 350, and actuator 380.
• Introducer may include a plurality of housing portions, such as first housing portion (not shown) and a second housing portion 322 defining an inner volume, optionally an inner volume including first inner volume portion 318a and second inner volume portion 318b.
• Actuator 380 may include a first portion 381, second portion 385, and wall 387 connecting first portion 381 and second portion 385.
• medical device 300 may also include one or more features described in other embodiments, for example a secondary catheter and a lock (optionally with a blunt cannula) at distal end thereof.
• medical device 300 further may include a plurality of flexible members, in the form of flexible fibers 324.
• Flexible fibers 324 may be connected with introducer 310 through friction fit, ultrasonic weld, adhesives, or combinations thereof.
• Flexible fibers 324 may be formed of any suitable material capable of limiting deflection of catheter 350.
• flexible fibers 324 are formed of a silicone-containing material.
• flexible fibers 324 are arranged within inner volume of introducer 310, for example in second inner volume 318b, in any suitable angular orientation.
• flexible fibers 324 are arranged substantially about a perimeter (e.g., circumference) of second inner volume portion 318b. In non-limiting embodiments, flexible fibers 324 are arranged within second inner volume portion 318b in a manner that substantially or completely surrounds catheter 350. As with other embodiments of flexible member disclosed herein, plurality of flexible fibers 324 may be formed of a material that allows flexible fibers 324 to maintain sufficient flexibility to allow flexible fibers 324 to be displaced by actuator 380 (e.g., wall 387) as actuator moves catheter 350 through inner volume of introducer 310. In non-limiting embodiments, flexible fibers 324 may be formed of a material with sufficient resiliency such that flexible fibers 324 return to their original orientation following transit of actuator 380, thereby limiting deflection of catheter 350 within inner volume of introducer 310.
• actuator 380 e.g., wall 387
• FIG. 12A shown is a cross-section view of an existing medical device 400.
• the inner volume of the medical device 400 is tortuous, and the configuration of actuator 480 matches this tortuous geometry, for example arrangement of wall 487. This arrangement can require a larger volume 418b surrounding a catheter (not shown), which can allow for greater deflection of a catheter or other medical implement during displacement thereof.
• Shown in FIG. 12B is a medical device 500 with a simplified inner geometry of introducer 510.
• the simplified inner geometry allows for a reduced volume 518b as compared to known devices (418b, as shown in FIG. 12A).
• FIG. 12A shows a reduced volume 518b as compared to known devices (418b, as shown in FIG. 12A).
• the simplified geometry allows for a simplified actuator 580, for example a linear, non-tortuous wall 587 connecting actuator first portion 581 with actuator second portion 585. While one non-limiting configuration of inner volume 518b is shown in FIG. 12B, those of skill will appreciate that various cross-sectional shapes can be accommodated, so long as the volume in which a catheter or other medical implement can be deflected is minimized.
• a barrier 524 for example such as a flexible member described herein, can be included, further limiting the ability of a medical implement, such as a displaceable catheter.
• introducer 510 with a simplified geometry includes a plurality of housing portions, for example as described herein.
• the simplified geometry may require the introducer housing portions to be connected with an ultrasonic weld or adhesive, rather than through a snap or friction fit as is possible with known devices, such as those shown in FIG. 12A.
• one or more additional elements for reducing deflection of a medical implement may be employed.
• one or more lubricants can be included within introducer interior, on an exterior surface of the medical implement, and/or both.
• the lubricant is a silicone-containing lubricant.
• the lubricant is a polydimethylsiloxane-containing lubricant.
• one or more additional supporting structures for example ribs, protrusions, or the like, may be included within introducer interior.
• introducer may be molded with one or more supporting structures.
• one or more supporting structures can be overmolded or attached to introducer through an adhesive, ultrasonic weld, or the like.

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• 2022
  • 2022-10-25 WO PCT/US2022/047641 patent/WO2023076204A1/en not_active Ceased
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  • 2022-10-25 EP EP22888028.2A patent/EP4422495A4/en active Pending
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