Medical Devices and Methods

US2016015267A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016015267-A1
Application numberUS-201514841224-A
CountryUS
Kind codeA1
Filing dateAug 31, 2015
Priority dateAug 31, 2009
Publication dateJan 21, 2016
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Methods and devices to monitor an analyte in body fluid are provided. Embodiments include continuous or discrete acquisition of analyte related data from a transcutaneously positioned in vivo analyte sensor automatically or upon request from a user.

First claim

Opening claim text (preview).

What is claimed is: 1 . An apparatus, comprising: an analyte sensor having a portion in fluid contact with bodily fluid under a skin surface and configured to generate signals corresponding to monitored analyte level in the bodily fluid, wherein the analyte sensor does not require user initiated calibration during the entire period of the analyte sensor usage life; a power supply; and sensor electronics operatively coupled to the analyte sensor and the power supply, the sensor electronics configured to receive the signals generated by the analyte sensor and to generate one or more data packets including the received signals from the analyte sensor; wherein the sensor electronics is configured to alternate drawing power from the power supply and from radio frequency (RF) power of a remote device positioned within a predetermined distance from the sensor electronics. 2 . The apparatus of claim 1 , wherein the sensor electronics is configured to disable a connection to the power supply when a predetermined level of RF power is detected. 3 . The apparatus of claim 2 , wherein the sensor electronics is powered by the RF power from the remote device to generate the one or more data packets. 4 . The apparatus of claim 2 , further including a switch connecting the power supply to the sensor electronics, wherein the switch is open when the predetermined level of RF power is detected such that the connection between the power supply and the sensor electronics is disabled. 5 . The apparatus of claim 4 , wherein the switch is closed when the predetermined level of RF power is no longer detected by the sensor electronics such that the sensor electronics is electrically connected to the power supply. 6 . The apparatus of claim 1 , further including a rechargeable power source operatively coupled to the sensor electronics, wherein when the remote device is positioned with a predetermined distance from the sensor electronics, the RF power from the remote device charges the rechargeable power source. 7 . The apparatus of claim 1 , wherein the bodily fluid includes one of dermal fluid or interstitial fluid. 8 . The apparatus of claim 1 , wherein the analyte sensor includes a plurality of electrodes including a working electrode comprising an analyte-responsive enzyme bonded to a polymer disposed on the working electrode. 9 . The apparatus of claim 8 , wherein the analyte-responsive enzyme is chemically bonded to the polymer disposed on the working electrode. 10 . The apparatus of claim 8 , wherein the working electrode comprises a mediator bonded to the polymer disposed on the working electrode. 11 . The apparatus of claim 10 , wherein the mediator is crosslinked with the polymer disposed on the working electrode. 12 . The apparatus of claim 1 , wherein the analyte sensor includes a plurality of electrodes including a working electrode comprising a mediator bonded to a polymer disposed on the working electrode. 13 . The apparatus of claim 1 , wherein the entire period of the analyte sensor usage life corresponds to the time period of monitoring the analyte level in the bodily fluid, and starts when the sensor electronics is activated, and ends when the sensor electronics is deactivated. 14 . The apparatus of claim 13 , wherein the sensor electronics is deactivated when no additional signals from the analyte sensor is processed by the sensor electronics. 15 . The apparatus of claim 1 , further including a data storage unit for storing an identification information and analyte sensor calibration information. 16 . The apparatus of claim 15 , wherein the sensor electronics is operatively coupled to the data storage unit, and the generated one or more data packets include the identification information and the analyte sensor calibration information.

Assignees

Inventors

Classifications

  • Means for recording calibration data · CPC title

  • Social work or social welfare, e.g. community support activities or counselling services · CPC title

  • for measuring glucose, e.g. by tissue impedance measurement · CPC title

  • Monitoring a patient using a global network, e.g. telephone networks, internet · CPC title

  • for local operation · CPC title

Patent family

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Frequently asked questions

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What does patent US2016015267A1 cover?
Methods and devices to monitor an analyte in body fluid are provided. Embodiments include continuous or discrete acquisition of analyte related data from a transcutaneously positioned in vivo analyte sensor automatically or upon request from a user.
Who is the assignee on this patent?
Abbott Diabetes Care Inc
What technology area does this patent fall under?
Primary CPC classification A61B5/0017. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Jan 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).