Analyte sensor
The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.
1. An analyte monitoring system comprising:
a first component comprising:
a transcutaneous analyte sensor having an in vivo portion and an ex vivo portion, wherein the transcutaneous analyte sensor is configured to measure a signal indicative of analyte concentration in a host;
electrical contacts operably connected to the transcutaneous analyte sensor,
wherein the first component is associated with a sensor code, wherein the sensor code is associated with calibration information, and wherein the calibration information enables calibration of sensor data without requiring a reference analyte measurement during sensor use; and
a second component separate from the first component, wherein the second component comprises:
sensor electronics configured to be operably connected to the transcutaneous analyte sensor through the electrical contacts of the first component when the second component is attached to the first component by the host, wherein the sensor electronics are configured to wirelessly communicate with a receiver, and wherein the second component is associated with the sensor code.
2. The analyte monitoring system of claim 1 , wherein the first component and the second components are both labeled with the sensor code.
3. The analyte monitoring system of claim 2 , wherein at least one of the first component and the second component comprise a package, and wherein the package is labeled with the sensor code.
4. The analyte monitoring system of claim 3 , wherein the sensor code is alphanumeric.
5. The analyte monitoring system of claim 1 , wherein the sensor code is alphanumeric.
6. The analyte monitoring system of claim 1 , wherein the second component is configured to transmit information associated with the sensor code to the receiver.
7. The analyte monitoring system of claim 1 , wherein the electrical contacts are operably connected to the ex vivo portion of the transcutaneous sensor.
8. The analyte monitoring system of claim 1 , wherein the first component comprises a contact holder.
9. The analyte monitoring system of claim 8 , wherein the first component comprises a seal located over at least a portion of the contact holder.
10. The analyte monitoring system of claim 9 , wherein the seal at least partially surrounds the ex vivo portion of the transcutaneous sensor.
11. The analyte monitoring system of claim 9 , wherein the seal at least partially surrounds the electrical contacts.
12. The analyte monitoring system of claim 1 , wherein the transcutaneous analyte sensor is radiation sterilized.
13. The analyte monitoring system of claim 12 , wherein the sensor electronics are not radiation sterilized.
14. The analyte monitoring system of claim 1 , further comprising an applicator.
15. The analyte monitoring system of claim 14 , wherein one or both of the first component and the second component is coupled to the applicator.
16. The analyte monitoring system of claim 14 , wherein the first component comprises a mounting unit operably connectable to the transcutaneous analyte sensor.
17. The analyte monitoring system of claim 1 , wherein the first component comprises a mounting unit operably connectable to the transcutaneous analyte sensor.
18. The analyte monitoring system of claim 17 , wherein the mounting unit is operably connected to the applicator.
19. The analyte monitoring system of claim 14 , wherein the applicator and the first component are configured to be operably connected by the host prior to the start of the sensor use.
20. The analyte monitoring system of claim 1 , wherein the calibration information associated with the sensor code is stored in the sensor electronics.
21. The analyte monitoring system of claim 1 , wherein the sensor electronics are attachable to multiple different sensors.