WO2018110716A1 - Appareil médical mobile et procédé pour le faire fonctionner - Google Patents

Appareil médical mobile et procédé pour le faire fonctionner Download PDF

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Publication number
WO2018110716A1
WO2018110716A1 PCT/KR2016/014512 KR2016014512W WO2018110716A1 WO 2018110716 A1 WO2018110716 A1 WO 2018110716A1 KR 2016014512 W KR2016014512 W KR 2016014512W WO 2018110716 A1 WO2018110716 A1 WO 2018110716A1
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WO
WIPO (PCT)
Prior art keywords
user
medical device
mobile medical
analysis
applications
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PCT/KR2016/014512
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English (en)
Korean (ko)
Inventor
윤승용
김용재
이보경
Original Assignee
(주)비비비
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Application filed by (주)비비비 filed Critical (주)비비비
Priority to PCT/KR2016/014512 priority Critical patent/WO2018110716A1/fr
Priority to KR1020167035126A priority patent/KR20180081854A/ko
Publication of WO2018110716A1 publication Critical patent/WO2018110716A1/fr

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    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04MTELEPHONIC COMMUNICATION
    • H04M1/00Substation equipment, e.g. for use by subscribers
    • H04M1/72Mobile telephones; Cordless telephones, i.e. devices for establishing wireless links to base stations without route selection
    • H04M1/724User interfaces specially adapted for cordless or mobile telephones
    • H04M1/72403User interfaces specially adapted for cordless or mobile telephones with means for local support of applications that increase the functionality
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/14532Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/145Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue
    • A61B5/1455Measuring characteristics of blood in vivo, e.g. gas concentration, pH value; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid, cerebral tissue using optical sensors, e.g. spectral photometrical oximeters
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04MTELEPHONIC COMMUNICATION
    • H04M1/00Substation equipment, e.g. for use by subscribers
    • H04M1/02Constructional features of telephone sets
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04MTELEPHONIC COMMUNICATION
    • H04M1/00Substation equipment, e.g. for use by subscribers
    • H04M1/02Constructional features of telephone sets
    • H04M1/0202Portable telephone sets, e.g. cordless phones, mobile phones or bar type handsets
    • H04M1/026Details of the structure or mounting of specific components
    • H04M1/0274Details of the structure or mounting of specific components for an electrical connector module
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04MTELEPHONIC COMMUNICATION
    • H04M1/00Substation equipment, e.g. for use by subscribers
    • H04M1/72Mobile telephones; Cordless telephones, i.e. devices for establishing wireless links to base stations without route selection
    • H04M1/725Cordless telephones
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04MTELEPHONIC COMMUNICATION
    • H04M2201/00Electronic components, circuits, software, systems or apparatus used in telephone systems
    • H04M2201/34Microprocessors
    • HELECTRICITY
    • H04ELECTRIC COMMUNICATION TECHNIQUE
    • H04MTELEPHONIC COMMUNICATION
    • H04M2201/00Electronic components, circuits, software, systems or apparatus used in telephone systems
    • H04M2201/38Displays

Definitions

  • Embodiments of the present invention relate to mobile medical devices and methods of operation thereof.
  • Mobile medical devices can measure / analyze various biomarkers such as blood sugar, blood pressure, and cholesterol, and are portable and easy to use, so users can easily use them at home without having to visit the hospital every time.
  • Biomarkers that can be measured / analyzed by mobile medical devices are very diverse, including sugars, lactic acid, hemoglobin, triglycerides, total cholesterol, LDL cholesterol, and HDL cholesterol. Diabetes, anemia, cardiovascular, gout, cancer, pregnancy, drug addiction and so many kinds.
  • the mobile medical device can provide an application that can measure / analyze by biomarkers and diseases.
  • a user may use the mobile medical device to measure / analyze a plurality of diseases or biomarkers.
  • a user may have multiple applications, for example, if a patient has more than one disease, or if a nurse in the hospital measures / analyzes the diseases of patients he or she manages. have.
  • each application when using a conventional mobile medical device, each application is only implemented / implemented independently, it is not interworking between applications. For example, if a user wants to use several applications, the user has to perform a login procedure for each application individually. In addition, after all mobile medical devices had been used, the logout procedure also had to be performed on a per-application basis.
  • One embodiment of the present invention is a technical object that a user can log in / log out to a plurality of analysis applications used by the user through a single login / logout procedure.
  • a mobile medical device includes: a housing in which a port into which a biosensor is inserted is formed; A memory disposed inside the housing, the memory storing account management software for managing a plurality of analysis applications and a user's account; And a processor disposed inside the housing to control the plurality of analysis applications and the account management software, wherein the processor controls the account management software when the login request is input from the user. If the authentication process is successful and the user is successfully authenticated, the user logs in a batch log-in process for the plurality of coordinated applications included in the list of coordinated applications corresponding to the user among the plurality of analysis applications, and the batch login is performed. By controlling any one of a plurality of processed interlocking applications, the analysis data for the body fluid sample accommodated in the biosensor inserted through the port is generated.
  • the present invention may further include a measurement module for measuring the value of the target biomarker (Target Biomarker) from the body fluid sample.
  • Target Biomarker Target Biomarker
  • the processor identifies the biosensor inserted through the port after the batch login process is completed, and if the identified biosensor does not match any of the plurality of interlocking applications, the At least one of an operation of outputting a warning message and an operation of logging out the user may be performed by controlling an account management software.
  • the processor identifies a biosensor inserted through the port, executes an analysis application corresponding to the identified biosensor among the plurality of analysis applications, and executes the executed analysis application.
  • the account management software may be controlled to proceed with the authentication process.
  • the processor controls the account management software to change the request.
  • the coordinated application list may be changed based on the content of the.
  • the linked application list is generated based on user payment information, and when the user payment information of the logged-in user is changed, the processor adds the linked application list to the linked application list based on the changed user payment information.
  • the interlocking application included can be changed.
  • the processor controls the account management software to inform all of the plurality of coordinated applications included in the coordinated application list corresponding to the user.
  • the authentication result value for the user may be transmitted, and the plurality of coordinated applications may be controlled to log in the user.
  • the processor when the processor performs a batch login process, when the authentication for the user is successful, the plurality of analysis applications are controlled, and each of the plurality of analysis applications is included in the coordinated application list.
  • the application for analysis which is determined to be included in the linked application list, may log in the user.
  • the processor controls the account management software to read user-specific environment information from the memory or receive from an external server, and log-in based on the user-specific environment information. It is possible to provide a customized user interface for a given user.
  • the processor may control the measurement module to operate the measurement module in a measurement standby mode for a preset time.
  • the memory further stores user distance measurement software
  • the processor executes the user distance measurement software so that the mobile medical device when the distance between the user and the mobile medical device exceeds a preset value.
  • the device can be controlled in secure mode.
  • a user may collectively log in / log out to a plurality of analysis applications to be used through one login / logout procedure.
  • a personalized service may be provided to a user based on characteristics of a mobile medical device or a biosensor, a user's disease, history information, and the like.
  • FIG. 1 is a diagram illustrating a mobile medical device according to an exemplary embodiment.
  • FIG. 2 illustrates a mobile medical device having a plurality of ports according to an embodiment.
  • FIG. 3 is a diagram illustrating a mobile medical device and an auxiliary device, according to an exemplary embodiment.
  • FIG. 4 is a diagram illustrating a mobile medical device in which a measurement module according to an embodiment may be detachable.
  • 5 and 6 are diagrams illustrating a plurality of analysis applications according to an exemplary embodiment.
  • FIG. 7 is a diagram illustrating a linked application list, according to an exemplary embodiment.
  • FIGS. 8 and 9 are diagrams illustrating an embodiment of use of a mobile medical device according to one embodiment.
  • FIG. 10 is a diagram illustrating a configuration of a mobile medical device according to one embodiment.
  • FIG. 11 is a flowchart of a method of operating a mobile medical apparatus, according to an exemplary embodiment.
  • FIG. 1 is a diagram illustrating a mobile medical device 100 according to an embodiment.
  • the mobile medical device 100 may be a portable device for analyzing or diagnosing a health condition or a disease of a user.
  • a port 120 into which the biosensor 101 may be inserted may be formed in the housing 110 of the mobile medical device 100, and the biosensor 101 may be formed.
  • the port 120 may be inserted into the mobile medical device 100.
  • the biosensor 101 may be a device for measuring biometric information of a user.
  • the biosensor 101 may be in the form of a strip, but is not limited thereto.
  • the user may put a body fluid sample such as blood, saliva, or urine into the biosensor 101, insert the biosensor 101 containing the body fluid sample into the mobile medical device 100, and then perform a mobile medical care.
  • a body fluid sample can be analyzed by executing an analysis application installed in the device 100.
  • the analysis result of the mobile medical device 100 for the bodily fluid sample may be based on the value of a specific biomarker (e.g., the amount of glucose in the blood, the value of blood pressure, etc.), the presence or absence of a disease or health condition (e.g. Confirmation of pregnancy, etc.), and the like.
  • a specific biomarker e.g., the amount of glucose in the blood, the value of blood pressure, etc.
  • a disease or health condition e.g. Confirmation of pregnancy, etc.
  • the biosensor 101 may have a different detailed structure, such as its structure or size, or a measurement method applied according to a target biomarker or a disease to be detected.
  • the mobile medical device 100 according to an embodiment may have a variety of modification structure, to be compatible with the various biosensor 101 as described above.
  • an embodiment of a mobile medical device 100 having various shapes / structures will be described with reference to FIGS. 2 to 4.
  • FIG. 2 is a diagram illustrating a mobile medical device 100 having a plurality of ports according to an embodiment.
  • the mobile medical device 100 may include a plurality of ports 210, 220, and 230 to accommodate various biosensors.
  • the first port 210 may have a structure capable of receiving the biosensor 201 to which an electrochemical analysis method is applied.
  • the first port 210 has a hole in which the biosensor 201 can be inserted, and the hole physically supports the biosensor 201 so that the biosensor 201 is not shaken or removed after the biosensor 201 is inserted. It can have a size and shape that can be given.
  • the mobile medical device 100 may further include a first measurement module (not shown) for analyzing the biosensor 201 to which an electrochemical analysis method inserted into the housing through the first port 210 is applied.
  • the first measurement module may be disposed inside the housing to be adjacent to the first port 210.
  • the first measurement module may have a hardware structure including one or more electrodes to perform an electrochemical analysis. Through this hardware structure, the first measurement module according to an embodiment may receive an electrical signal through electrical switching from the biosensor 201 through an electrode.
  • the first measurement module may measure a value of a target biomarker from the biosensor 201 inserted through the first port 210 through the received electrical signal.
  • the first measurement module in addition to the value of the target biomarker, various information (for example, information on the type of the biosensor 201, information on whether the biosensor 201 is inserted, Calibration information for correcting the measured value, etc.) can be obtained from the biosensor 201.
  • the operation of the first measurement module may include software for controlling the operation of the first measurement module stored in a memory included in the mobile medical device 100 according to an embodiment. Can be performed by controlling.
  • the first measurement module may include a separate memory and a processor, and software for controlling the operation of the first measurement module is stored in a memory provided in the first measurement module, and the corresponding software is provided in the first measurement module. It can be controlled by a processor.
  • the second port 220 may have a structure that can accommodate the biosensor 202 to which the reflected light analysis method is applied.
  • the second port 220 may have a structure (drawer structure) in which an adapter or a tray is received in a sliding manner in a space inside a housing of the mobile medical device 100.
  • the biosensor 202 may be accommodated by being placed or inserted into one side of the adapter or tray.
  • the adapter or the tray is slid into the housing, so that the biosensor can be measured under the dark room environment formed inside the housing.
  • the mobile medical device 100 may further include a second measurement module (not shown) for analyzing the biosensor 202 to which the reflected light analysis method inserted into the housing through the second port 220 is applied.
  • the second measurement module can be disposed inside the housing to be adjacent to the second port 220.
  • the second measurement module may have a hardware structure including a light emitting device (eg, an LED array, etc.) and a light receiving device (eg, a camera, a photodetector, etc.) to perform reflected light analysis.
  • the second measurement module may irradiate light to the biosensor 202 inserted through the second port 220 through the light emitting device, and sense light reflected from the biosensor 202 through the light receiving device. .
  • the second measurement module may measure a value of the target biomarker from the biosensor 202 inserted through the second port 220.
  • the second measurement module not only the value of the target biomarker, but also various information (for example, information on the type of the biosensor 202, information on whether the biosensor 202 is inserted, and a measurement value). Calibration information, etc.) may be obtained from the biosensor 202.
  • the operation of the second measurement module may include software for controlling the operation of the second measurement module stored in the memory included in the mobile medical device 100 according to an embodiment. Can be performed by controlling.
  • the second measurement module may have a separate memory and a processor, and the software for the second measurement module is stored in a memory provided in the second measurement module, and the software is provided by a processor provided in the second measurement module. Can be controlled.
  • the mobile medical device 100 may include a third port 230 (third measurement module) and a fourth port.
  • a port (fourth measurement module) etc. can be further provided.
  • the third port 230 may be targeted to the biosensor 202 to which the reflectance analysis method is applied, similarly to the second port 220, but is different from the second port 220. It may have a different physical structure or size.
  • the third port 230 may be hardware compatible with the biosensor 203 to which an analysis method other than an electrochemical analysis method or a reflection intensity analysis method (for example, an analysis method according to enzyme-linked immunosorbent absorption method) is applied. It can be connected to the corresponding measuring module with the corresponding structure.
  • FIG. 3 illustrates a mobile medical device 100 and an auxiliary device, according to an exemplary embodiment.
  • a separate auxiliary device 310 coupled to the mobile medical device 100 may be connected to the mobile medical device 100.
  • the mobile medical device 100 may be provided together, and thus, the mobile medical device 100 may have a structure that may be physically separated / coupled with the auxiliary device 310.
  • the mobile medical device 100 may additionally secure a port into which the biosensor may be inserted through the separate auxiliary device 310, and further secure the types of compatible biosensors.
  • a separate auxiliary device 310 coupled to the mobile medical device 100 may be used physically separated from the mobile medical device 100, but the technical description of the port, measurement module, account management method, etc. Features may be equally applied to a separate auxiliary device 310.
  • FIG. 4 is a diagram illustrating a mobile medical device 100 in which a measurement module according to an embodiment may be detachable.
  • the mobile medical device 100 may be compatible with various biosensors
  • a portion of the peripheral portion of the port 410 in the mobile medical device 100 may be moved to the dongle 420.
  • the mobile medical device 100 may have a structure in which the dongle 420 may be physically separated / coupled from the mobile medical device 100.
  • the dongle 420 may include a measurement module to which (1) a port 410 having a different physical structure for each biosensor and (2) a measurement method corresponding to each biosensor is applied to various biosensors. Accordingly, the user of the mobile medical device 100 may exchange the dongle 420 from the mobile medical device 100 according to a purpose or a biosensor.
  • the description of the housing, port, measurement module, and biosensor of the mobile medical device 100 described above with reference to FIGS. 1 to 4 may be separately applied to one mobile medical device 100, as well as two. More than one may apply.
  • the mobile medical device 100 may install an analysis application for analyzing the biosensor.
  • the mobile medical device 100 since the biomarker or disease that the user wants to analyze through the mobile medical device 100 may vary depending on the user, the mobile medical device 100 may be provided with a plurality of analysis applications.
  • a plurality of analysis applications will be described in more detail with reference to FIGS. 5 and 6.
  • 5 and 6 are diagrams illustrating a plurality of analysis applications according to an exemplary embodiment.
  • an analysis application for each biomarker may be installed in the mobile medical device 100.
  • an application 505 for measuring / analyzing triglyceride may be provided as an analysis application.
  • an analysis application for each disease may be installed in the mobile medical device 100.
  • An application 605 for analyzing / diagnostics may be provided as an analysis application.
  • the analysis application described in FIGS. 5 and 6 is only an example, and the present disclosure is not limited to providing an analysis application classified by disease or biomarker.
  • the user may log in with his or her account in order to use the analysis application installed in the mobile medical device 100.
  • the user may acquire the authority to use the analysis application by logging in, and may store and manage his / her own measurement / analysis results in his / her account information.
  • the user may log out. By logging out, the user can prevent leakage of information such as usage results or usage history of the analysis application.
  • the login / logout procedure for the mobile medical device 100 of the user may be performed by account management software installed in the mobile medical device 100.
  • the account management software is stored in the memory of the mobile medical device 100 and may be controlled by the processor of the mobile medical device 100.
  • the account management software may collectively log in / log out a user for a plurality of analysis applications. Therefore, even if a user needs to use two or more analysis applications, the user can use the analysis applications that he / she wants to use through one login / logout. For example, when the account management software requests a login / logout request for a plurality of analysis applications from the user, the account management software may collectively log in / log out the user for the requested plurality of analysis applications. Alternatively, when the account management software requests a login / logout request for any one analysis application from the user, the account management software may log in / collect the user collectively for the other analysis applications that the user may use together with the requested analysis application. You can log out.
  • An interlocked application list may be set for each user for batch login / logout.
  • the coordinated application list may be a list of analysis applications that the user has permission to use.
  • the coordinated application included in the coordinated application list may be set or changed by the user.
  • a user having administrator authority for the mobile medical apparatus 100 may set or change a user-specific linked application list.
  • the administrator changes, deletes, or adds the linked application list by changing the contents of the list (for example, changing the list of included analysis applications). And so on.
  • the user may be required to pay a usage fee for using the mobile medical device 100.
  • the usage amount may have a plurality of detailed plans, and the type / number of analysis applications that can be used according to the contents may be set differently.
  • the coordinated application list may be set according to the payment details of the user.
  • the type or number of analysis applications included in the user's linked application list may be set differently according to the user's payment history, or the number or type of menus or functions available to the user may be set differently even for the same analysis application. Can be. Therefore, when the payment information of the user is changed, the processor of the mobile medical apparatus 100 may change the coordinated application included in the coordinated application list based on the changed user payment information.
  • a plan such as Table 1 below may be applied to the mobile medical device 100.
  • User 1 has a plan Lv.
  • the user 1 may select up to two applications required by the user from among a plurality of analysis applications installed in the mobile medical device 100, in which case one analysis application selected by the user 1 Alternatively, two may be included in the coordinated application list for user 1.
  • the account management software may generate a linked application list including one or two analysis applications selected by the user, and may store the generated list by matching the user 1.
  • plan Lv. User 2 who selects 2 can register an additional person as a user, but in this case, since the additional user cannot individually select the analysis application to be used, the linked application list for the additional user is It can be set equal to the list.
  • the mobile medical device 100 may recommend to the user a customized list including analysis applications suitable for the user based on these various factors.
  • the memory of the mobile medical apparatus 100 may store a customized list recommendation software, and the processor of the mobile medical apparatus 100 may generate a customized list for each user by controlling the customized list recommendation software. I can recommend it to Alternatively, the mobile medical apparatus 100 may receive a customized list generated by an external server and recommend it to a user.
  • the coordinated application list or the customized list may be stored in the memory of the mobile medical device 100 or in an external server.
  • the right to access the linked application list may be set differently for each software or analysis application stored in the mobile medical apparatus 100.
  • the account management software may have a right to access the linked application list.
  • all or a part of the plurality of analysis applications installed in the mobile medical device 100 may have a right to access the linked application list.
  • which analysis application may have access to the list may be set and changed by a user or an administrator of the mobile medical apparatus 100.
  • the account management software may grant access rights to all or part of the plurality of analysis applications installed in the mobile medical device 100.
  • the account management software informs all or part of a plurality of analysis applications installed in the mobile medical device 100 of a look-up table existing in a specific area, and the whole or part of the linked application through the look-up table. You can make the list accessible.
  • FIG. 7 is a diagram illustrating a linked application list, according to an exemplary embodiment.
  • a plurality of analysis applications may be installed in the mobile medical device 100.
  • the user may set a linked application list by selecting some analysis applications from all the analysis applications installed in the mobile medical apparatus 100.
  • the coordinated application list for the user 1 may include the first analysis application 701 and the second analysis application 702.
  • the second, third, and fourth analysis applications 702, 703, and 704 due to the nature of the disease
  • the coordinated application list 720 may be set to include 704.
  • the batch login operation of the account management software will be described.
  • the account management software performs authentication on the user 2
  • If the authentication is successful not only the user 2 is logged in to the second analysis application 702 but also the third and fourth analysis applications 703 and 704 included in the linked application list 720 for the user 2.
  • the user 2 may perform the third and fourth analysis applications 703 as well as the second analysis application 702 with only one login, without having to log in again to use the third and fourth analysis applications 703 and 704. 704) can be used.
  • the account management software may proceed with the authentication process for the user when a login request is input from the user.
  • a user's login request may be input by the user executing one of the analysis applications and selecting a login menu from a menu of the executed analysis application (such as touching a touch screen).
  • the account management software may execute a login window in response to the insertion of the biosensor so that the user can log in more conveniently.
  • the biosensor may be logged in after the biosensor is inserted into the mobile medical device 100, or after the biosensor is inserted in the mobile medical device 100. If the user inserts the biosensor into the mobile medical device 100 before the user is logged in, (2-1) launches a login window provided by the account management software, or (2-2).
  • a login window provided by an application corresponding to the inserted biosensor among a plurality of analysis applications (if there are a plurality of corresponding applications, any one may be selected) may be executed. For example, when a user inserts a blood glucose measurement biosensor into the mobile medical device 100, a login window may be displayed while an application for analyzing blood glucose or diabetes is executed.
  • authentication information (user ID, password, fingerprint information, etc.) for the user used in the authentication procedure may be stored in the memory of the mobile medical device 100, in which case the account The management software may perform an authentication procedure for the user by comparing the authentication information of the user stored in the memory with the information input when the user requests the login.
  • the authentication information for the user may be stored in an external server, and in this case, the account management software transmits the information input when the user logs in to the external server by using the communication function of the mobile medical device 100, and the external server.
  • the authentication procedure for the user can be performed by receiving the authentication result value from the user.
  • a location, an area, etc. in which the mobile medical device 100 can be used may be limited for each user. For example, if the mobile medical device 100 is paid for a nurse, the user (nurse) is set to use the mobile medical device 100 only when the mobile medical device 100 is within a preset distance from the hospital. Can be.
  • the mobile medical device 100 may measure the position of the mobile medical device 100.
  • the mobile medical device 100 may measure the location of the mobile medical device 100 using the onboard GPS function.
  • the account management software may also consider the measured position value of the mobile medical device 100 when performing the authentication procedure. For example, the account management software may check whether the measured location of the mobile medical device 100 satisfies a predetermined criterion, and if it is determined that the measured medical care device deviates from the predetermined criterion, the account management software may not allow the user to log in regardless of the authentication result. You may not. When it is confirmed that the predetermined criteria are satisfied, the user may not process or allow the login according to the authentication result.
  • the account management software may call the linked application list corresponding to the user.
  • the linked application list may be stored in a memory of the mobile medical device 100, and in this case, the account management software may call the linked application list from the memory of the mobile medical device 100.
  • the linked application list may be stored in an external server, and in this case, the account management software may receive the linked application list from the external server by using the communication function of the mobile medical apparatus 100.
  • the account management software may collectively log-in the user for a plurality of coordinated applications included in the coordinated application list.
  • the account management software may transmit an authentication result value indicating that authentication of the user is successful to all of the plurality of coordinated applications included in the coordinated application list, and the plurality of coordinated applications receive the authentication result value, respectively. You can handle the login procedure for the user.
  • the account management software may verify the user's payment history.
  • the payment details may be stored in a memory or an external server of the mobile medical apparatus 100, and the account management software may receive the payment details from the memory or an external server and proceed with the verification of the payment details.
  • the account management software compares the list of linked applications for the user with the billing details and the user's rights for each of the billing details, and when it is confirmed that the user has permission to use all the linked applications on the list of linked applications. Only one batch login process can be performed.
  • the account management software may either (1) print a warning message to the user, (2) disallow the user's login procedure, or ( 3) A message for guiding the user with customized payment information may be output and provided to the user.
  • each of the plurality of analysis applications installed in the mobile medical apparatus 100 checks whether the user is included in the linked application list to perform a batch login operation. Can be.
  • the analysis application may request a linked application list from the account management software. In this case, upon receiving the linked application list from the account management software, the analysis application may check whether the received linked application list is included in the list.
  • the analysis application inquires whether it is included in the linked application list by the account management software, and receives the result of whether it is included in the list by the account management software. You can check it.
  • (3) in the case of the analysis application having the access right to the linked application list the linked application list may be directly called and the self-listed application list may be checked.
  • the analysis application may log in the user.
  • the successful authentication of the user can be confirmed by (1) the account management software sending an authentication success message to the analysis application, or (2) the analysis application asking the account management software about the authentication result.
  • the analysis applications included in the list may log in the user in parallel, thereby processing a batch login procedure for the user.
  • the batch login / logout operation of the mobile medical device 100 may be utilized not only when there is one user of the mobile medical device 100 but also when there are several users who use one mobile medical device 100. have.
  • FIG. 8 several family members may use one mobile medical device 100 in one home. Since the users of the mobile medical device 100 live in a home, one mobile medical device 100 may be jointly used.
  • member 1 801 and member 2 802 use one mobile medical device 100
  • member 1 801 uses a batch login function to use mobile medical device 100. You can log in to multiple analysis applications you want to use at once.
  • the member 2 802 may use the mobile medical device 100
  • the member 1 801 may log in using the batch logout function. You can log out of multiple analysis applications at once.
  • one mobile medical device 100 in one hospital may be used by multiple nurses.
  • the nurse 1 910 may use the mobile medical device 100 to measure / analyze the health or disease state of the patients 911, 912, and 913 managed by the nurse 1 910. This allows patients to log in once to the required analytical applications.
  • the user who uses the mobile medical device 100 becomes nurse 1 901, but the measurement / analysis object may be patients 911, 912, and 913. Therefore, in this case, the account management software may store and manage not only information about the user but also information about the patient to be analyzed.
  • the nurse 1 901 provides a batch logout function so that the next nurse 2 902 can use the mobile medical device 100. You can log out at a time from any analytical application you logged in with.
  • the account management software may read out user-specific environment information from the memory of the mobile medical apparatus 100 or receive it from an external server.
  • the user-specific environment information may be information stored in a user interface set by the user or recommended to the user.
  • the user-specific environment information may be stored in a memory of the mobile medical apparatus 100 or may be stored in an external server.
  • the account management software may read environment information about the logged-in user from the user-specific environment information, and provide a customized user interface for the logged-in user based on the read environment information.
  • the customized user interface may display only the analysis application available to the user on the operating system of the mobile medical device 100, or may include information on how to arrange the displayed analysis application.
  • the mobile medical device 100 may operate in a measurement standby mode.
  • the measurement standby mode may be a state in which an analysis application and other necessary functions of the mobile medical device 100 are activated to enable the user to use the mobile medical device 100.
  • the target that remains activated may be set differently.
  • the measurement standby mode may be set such that all functions of the mobile medical device 100 remain active.
  • the measurement standby mode may be set to keep the measurement module active.
  • the mobile medical apparatus 100 may maintain the measurement standby mode when at least one analysis application is maintained in the logged in state.
  • the mobile medical device 100 may change the operation state from the measurement standby mode to the sleep mode.
  • the sleep mode may be a state in which the functions for measuring the biosensor by the mobile medical device 100 are dormant.
  • the dormant object may be set differently.
  • the sleep mode may be set such that all functions of the mobile medical device 100 are in a dormant state.
  • the sleep mode may be set such that only the measurement module is in the dormant state. By entering the sleep mode, the mobile medical device 100 may reduce power consumption.
  • the user can analyze / diagnose the bodily fluid sample using the linked application that has been logged in.
  • the linked application that has been logged in may be executed by the user's selection (for example, when the user touches one of the linked applications, etc.) or the linked application that has been logged in corresponding to the inserted biosensor may be automatically executed. Such automatic execution may be controlled by an operating system or account management software of the mobile medical device 100.
  • the executed interlocking application allows the user to analyze the body fluid sample received in the biosensor. That is, the coordinated application may generate analysis data by analyzing a body fluid sample.
  • the analytical data may be a value of a target biomarker included in a bodily fluid sample, or may be an analysis result of a disease or a health condition based on the value of the biomarker.
  • the companion application may transmit analysis data generated by analyzing a body fluid sample to an external server.
  • the external server may generate secondary analysis / diagnostic data using the analysis data received from the mobile medical apparatus 100 and transmit the generated secondary analysis / diagnostic data to the mobile medical apparatus 100.
  • the coordinated application may provide the secondary analysis / diagnosis data to the user through the display device of the mobile medical device 100. Therefore, the user can be provided with further analysis / diagnosis results as needed.
  • the mobile medical device 100 may operate in a security mode according to a distance from a user.
  • the mobile medical device 100 may store user distance measuring software for measuring distance to the user in a memory.
  • the user distance measurement software can measure the distance between the user and the mobile medical device 100. If the measured distance exceeds a preset value, the mobile medical device 100 may change the operation state to the security mode.
  • the security mode may be an operating state that prevents the use of all or part of the functions of the mobile medical device 100 or inquires about the measurement results of the analysis applications. The security mode may be released when the user is authenticated again.
  • the account management software or analysis application may log out the user when a logout request is input from the user.
  • the account management software may batch-logout a user from the corresponding analysis applications.
  • the account management software sends a logout request message to the analysis applications that are logged in, and the analysis applications that receive the logout request message log out the user. can do.
  • the logged-in analysis application or account management software may log out the user. have.
  • FIG. 10 is a diagram illustrating a configuration of a mobile medical apparatus 100 according to an embodiment.
  • the mobile medical device 100 may include a housing 1010, a processor 1030, and a memory 1040.
  • the housing 1010 may be a case surrounding the mobile medical device 100.
  • the memory 1040 and the processor 1030 may be arranged inside the housing 1010.
  • the port 1011 may be formed at a predetermined position of the housing 1010.
  • the biosensor 1001 may be inserted into the mobile medical device 100 through a port 1011 formed in the housing 1010.
  • one or more ports 1011 may be formed.
  • the port 1011 may be formed in an auxiliary device coupled to the mobile medical device 100, as shown in FIG. 3.
  • the port 1011 has been described in detail above with reference to FIGS. 1 to 4, and the following detailed description is replaced with the above description.
  • the mobile medical device 100 may further include a measurement module 1020.
  • One or more measurement modules 1020 may be formed.
  • the measurement module 1020 has been described in detail above with reference to FIGS. 1 to 4, and the following detailed description is replaced with the above description.
  • the mobile medical device 100 may be implemented in a smartphone such as a display device, a communication module, an input device, an output device (sound output, etc.), a GPS module, or a conventional mobile medical device 100. It may further include a device / module for implementing various functions.
  • the term 'device / module' may refer to an element in which a separate independent physical device such as a camera or a GPS chip is disposed in the housing 1010, or software mounted in the memory 1040 may include the processor 1030. When controlled and executed by the controller, this may mean a function / effect unit to be executed.
  • the account management software stored in the memory 1040 is controlled by the processor 1030 to implement the account management function
  • the function implemented as such may be referred to herein as an 'account management module'.
  • the memory 1040 may store a plurality of analysis applications for measuring / analyzing / diagnosing a bodily fluid sample and account management software for managing an account of a user.
  • the memory 1040 may include an operating system for operating the mobile medical device 100, software for controlling the measurement module 1020, customized list recommendation software, and login / log. Store out software, distance measurement software, and more.
  • the memory 1040 may store account information for each user, a linked application list for each user, authentication information for each user, usage history information for each user, and environment information for each user.
  • the memory 1040 may include information received from the measurement module 1020 (a value of the measured biomarker, information on the type of the biosensor 1001, and whether the biosensor 1001 is inserted). Information, calibration information for calibrating measured values, etc.), analysis data generated by an analysis application, and analysis / diagnosis data received from an external server.
  • the processor 1030 may execute or control a plurality of analysis applications and account management software stored in the memory 1040. In addition, all the software stored in the memory 1040 described above may be executed or controlled. In addition, operations of the mobile medical apparatus 100, the account management software, the analysis application, the coordinated application, and the various software described above with reference to FIGS. 1 to 9 may be controlled and performed by the processor 1030.
  • the processor 1030 may control the account management software to proceed with the authentication process for the user.
  • the processor 1030 may include information about which port 1011 is inserted into the biosensor 1001 or a type of biosensor 1001 inserted through the port 1011, a biosensor such as a manufacturer, and the like. Information about 1001) may be obtained. Therefore, based on this information, the processor 1030 may identify the biosensor 1001 inserted through the port 1011. For example, referring back to FIG. 2, when the first port 210 has a structure formed to accommodate the biosensor 201 to which the electrochemical analysis method is applied, the first port 210 is formed. When it is confirmed that the biosensor is inserted through, the processor 1030 may identify that the inserted biosensor is a biosensor 201 to which an electrochemical analysis method is applied.
  • the processor 1030 may identify that the inserted biosensor is the biosensor 202 to which the reflectance analysis method is applied. Such information acquisition and biosensor identification may be performed by an operating system or separate software of the mobile medical device 100 stored in the memory 1040.
  • the processor 1030 may execute an analysis application corresponding to the identified biosensor 1001 among the plurality of analysis applications. For example, when the inserted biosensor 1001 is identified as a blood glucose measurement biosensor, the processor 1030 may execute a blood sugar analysis application. At this time, the processor 1030 may control the application to activate the login menu window while the blood sugar analysis application is executed.
  • the analysis application corresponding to the biosensor 1001 is executed, the user may input a login request through the executed analysis application. For example, when the login menu window is activated and the blood sugar analysis application is executed, the user may request a login (for example, touching an 'OK' button after inputting an ID and password) using the activated login menu window.
  • the processor 1030 may control the account management software to proceed with the authentication process.
  • the processor 1030 may permit the use of the mobile medical device 100 only when the mobile medical device 100 is in a position within a preset range.
  • the memory 1040 may store location measurement software, and the processor 1030 may control the location measurement software to measure the location of the mobile medical device 100.
  • the processor 1030 determines whether the measured position value of the mobile medical apparatus 100 satisfies a preset criterion, and if it is determined that the measured value is out of the preset criterion, the processor 1030 controls the account management software (regardless of the authentication result). May not allow login. However, when it is determined that the predetermined criteria are satisfied, if the user is successfully authenticated, the processor 1030 may control the account management software to log in the user to the mobile medical apparatus 100.
  • the processor 1030 may control the account management software to call a list of coordinated applications corresponding to the user.
  • the processor 1030 may control the account management software to collectively log-in the user for a plurality of coordinated applications included in the coordinated application list.
  • the processor 1030 controls the account management software so that the authentication result value for the user is displayed to all of the plurality of coordinated applications included in the coordinated application list corresponding to the user. Can be transmitted.
  • the processor 1030 may control the plurality of coordinated applications, which have received the authentication result value, to log in the user.
  • the processor 1030 may check the plurality of analysis applications so that each of the plurality of analysis applications is included in the linked application list. Can be controlled.
  • the processor 1030 according to an exemplary embodiment (1) the analysis application requests the linked application list to the account management software, and the account management software lists the analysis application in response to the request.
  • the analysis application receiving the list may control the analysis application and the account management software so as to check whether the list is included in the list by referring to the list.
  • the processor 1030 inquires whether the analysis application is included in the linked application list by the account management software, and the account management software transmits a result of whether the analysis application is included in the analysis application in response to the inquiry.
  • the analysis application may control the analysis application and the account management software so as to check whether the analysis application is included in the list based on the received result.
  • the processor 1030 (3) in the case of the analysis application having access to the linked application list, the linked application list is called (accessed), and the analysis is performed to check whether it is included in the called linked application list. Application can be controlled.
  • the processor 1030 may control to log-in the user with respect to the analysis application determined to be included in the coordinated application list.
  • the processor 1030 may read out user-specific environment information from the memory 1040 or receive it from an external server. Upon obtaining the user-specific environment information, the processor 1030 may control the account management software to read the environment information on the logged-in user from the user-specific environment information. In addition, the processor 1030 may control the account management software to provide a customized user interface for the logged-in user based on the read environment information.
  • an object to log in to the mobile medical device 100 and an object to be analyzed may be different people.
  • the mobile medical device 100 is used in a hospital, the nurse logs in to the mobile medical device 100 with his account, but the subject of analysis will be a patient managed by the nurse.
  • the analysis target is an old elderly person
  • the target for logging in to the mobile medical device 100 may be one of family members who care for the old person.
  • the user-specific environment information may further include analysis target information matching the user-specific environment information.
  • the processor 1030 controls the account management software to provide a customized user interface for the logged-in user based on the read environment information. It may also provide information to be analyzed.
  • the processor 1030 may additionally provide information about a patient corresponding to the user. Therefore, the nurse may be provided with information about the patients who are actually using the mobile medical device 100. To this end, the processor 1030 may be
  • the mobile medical device 100 may operate in a measurement standby mode.
  • the processor 1030 may control the mobile medical device 100 such that all functions of the mobile medical device 100 remain active.
  • the mobile medical device 100 further includes the measurement module 1020
  • the processor 1030 operates in the measurement standby mode for a preset time.
  • Measurement module 1020 can be controlled to If the measurement module 1020 has a separate processor 1030, the processor 1030 transmits a signal instructing to operate in the measurement standby mode to the processor 1030 embedded in the measurement module 1020, The measurement module 1020 may control the measurement module 1020 to operate in the measurement standby mode for a preset time.
  • the mobile medical device 100 may change state to a sleep mode. For example, if none of the analytical applications remain logged in (e.g., all logged out), the processor 1030 may select all or preset target modules of the mobile medical device 100 in measurement standby mode. You can change the operating state to sleep mode. Or (2) when a preset time elapses from the time of login or a preset time elapses from the last use time of the user, the processor 1030 measures the entire or preset target module of the mobile medical device 100. The operating state can be changed from the standby mode to the sleep mode.
  • the processor 1030 may generate analytical data about the bodily fluid sample accommodated in the biosensor 1001 by controlling any one of the plurality of interlocked applications that are collectively logged in.
  • the user may insert the biosensor 1001 into the mobile medical device 100 after logging in.
  • the user may simply insert the biosensor after logging in first, or the user may insert a new biosensor to use the second and third biosensors.
  • the processor 1030 may identify the biosensor 1001 inserted through the port 1011 after the login process is completed. In addition, the processor 1030 may identify which of the plurality of coordinated applications included in the identified biosensor 1001 is included in the coordinated application list. When there is a matching interlocking application, the processor 1030 may execute the matching interlocking application so that the user may directly use the application without having to directly execute the corresponding application.
  • the processor 1030 may (1) Control to output a warning message, (2) control account management software or an analysis application to which the user is logged in, log out the user, or (3) purchase guidance message for the right to use the inserted biosensor. You can output
  • a user having administrator authority may set or change a user-specific linked application list.
  • a nurse using the mobile medical device 100 may be configured to have administrator rights for the accounts of the patients he manages, and a nurse with administrator rights may set or change the list of patients. have. If patient A has diabetes, the nurse needs to add an application for diabetic analysis to the list for patient A. In this case, after the nurse logs in to her account, the application for diabetic analysis is on the patient's list. You can set additional.
  • the processor 1030 may control the account management software to change the coordinated application list based on the contents of the change request. In addition, the processor 1030 may store the changed coordinated application list in the memory 1040.
  • the memory 1040 may further include user distance measurement software.
  • the processor 1030 may control user distance measurement software.
  • the processor 1030 may control the user distance measuring software to measure the distance between the user and the mobile medical device 100.
  • the processor 1030 may change the mobile medical device 100 to the security mode when the measured distance exceeds a preset value.
  • the processor 1030 may control the account management software to log out the user when a logout request is input from the user. When there are a plurality of analysis applications that are logged in, the processor 1030 may batch-logout a user from the corresponding analysis applications.
  • the processor 1030 may store the last usage information such as the last user, the last location, the last measurement time, etc. at the time of logout processing in the memory 1040.
  • the last usage information stored in this way may be (1) displayed on the display device when the mobile medical device 100 is used again, or (2) (if a schedule for a user who uses the mobile medical device 100 is set separately). It may be transmitted to a person who is determined as a user in a text message, an email, or the like, or (3) may be transmitted and stored to an external server so that it can be viewed using a separate communication device.
  • FIG. 11 is a flowchart of a method of operating a mobile medical apparatus, according to an exemplary embodiment.
  • a method of operating a mobile medical device may receive a login request from a user.
  • the method of operating the mobile medical device may control an account management software to proceed with an authentication procedure for the user (1110).
  • the method of operating the mobile medical device may call the list of coordinated applications corresponding to the user by controlling the account management software.
  • the method of operating the mobile medical apparatus may control the account management software to collectively log in the user for a plurality of linked applications included in the linked application list (1130).
  • the operation method of the mobile medical device controls the account management software to authenticate the user to all the plurality of coordinated applications included in the list of the coordinated applications corresponding to the user. You can send the result.
  • the operation method of the mobile medical device may control the plurality of coordinated applications that have received the authentication result value and log in the user.
  • the operation method of the mobile medical device includes a plurality of analysis applications such that each of the plurality of analysis applications checks whether or not they are included in the linked application list. You can control the application. If it is determined whether the list is included in the list, the operation method of the mobile medical apparatus may control to log-in the user for the analysis application which is confirmed to be included in the linked application list.
  • the operation method of the mobile medical device may generate analysis data on the bodily fluid sample accommodated in the biosensor by controlling any one of the plurality of interlocked applications that have been collectively logged in (1140). .
  • the operation method of the mobile medical device may log out the user by controlling the account management software when a logout request is input from the user.
  • the mobile medical apparatus may log out a user from the corresponding analysis applications.
  • Embodiments according to the present invention can be implemented in the form of program instructions that can be executed by various computer means can be recorded on a computer readable medium.
  • the computer readable medium may include program instructions, data files, data structures, etc. alone or in combination.
  • Program instructions recorded on the media may be those specially designed and constructed for the purposes of the present invention, or they may be of the kind well-known and available to those having skill in the computer software arts.
  • Examples of computer-readable recording media include magnetic media such as hard disks, floppy disks, and magnetic tape, optical media such as CD-ROMs, DVDs, and magnetic disks, such as floppy disks.
  • Examples of program instructions include not only machine code generated by a compiler, but also high-level language code that can be executed by a computer using an interpreter or the like.
  • the hardware device described above may be configured to operate as one or more software modules to perform the operations of the present invention, and vice versa.

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Abstract

L'invention concerne un appareil médical mobile et un procédé pour le faire fonctionner. Selon un mode de réalisation de la présente invention, un utilisateur peut se connecter à une pluralité d'applications d'analyse utilisées et se déconnecter de celles-ci de manière collective par une seule opération de connexion/déconnexion.
PCT/KR2016/014512 2016-12-12 2016-12-12 Appareil médical mobile et procédé pour le faire fonctionner WO2018110716A1 (fr)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002108823A (ja) * 2000-09-26 2002-04-12 Hitachi Ltd 本人認証方法、ワンストップサービス方法及び関連するシステム
KR20080071965A (ko) * 2008-07-16 2008-08-05 박명종 마우스를 이용한 단말기 보안 시스템 및 방법
WO2013032075A1 (fr) * 2011-08-26 2013-03-07 (주) 티엔피네트워크 Système et procédé de fourniture de services
KR20140006931A (ko) * 2011-01-31 2014-01-16 로베르트 보쉬 게엠베하 바이오마커 모니터링 장치 및 방법
KR20160128982A (ko) * 2016-10-31 2016-11-08 (주) 비비비 모바일 기반 체액 분석기 및 이를 포함하는 헬스케어 시스템

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005107984A (ja) * 2003-09-30 2005-04-21 Honda Motor Co Ltd ユーザ認証システム

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002108823A (ja) * 2000-09-26 2002-04-12 Hitachi Ltd 本人認証方法、ワンストップサービス方法及び関連するシステム
KR20080071965A (ko) * 2008-07-16 2008-08-05 박명종 마우스를 이용한 단말기 보안 시스템 및 방법
KR20140006931A (ko) * 2011-01-31 2014-01-16 로베르트 보쉬 게엠베하 바이오마커 모니터링 장치 및 방법
WO2013032075A1 (fr) * 2011-08-26 2013-03-07 (주) 티엔피네트워크 Système et procédé de fourniture de services
KR20160128982A (ko) * 2016-10-31 2016-11-08 (주) 비비비 모바일 기반 체액 분석기 및 이를 포함하는 헬스케어 시스템

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