Proteus Digital Health Feedback System SPC-2008
by Proteus Digital Health, Inc. United States GUDID
Product code DXH
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10856602005144 | Date2 Jul 2018 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Proteus Digital Health Feedback System
- Generic Name
- Medication adherence telemetric monitoring system, post-ingestion
- Model / Reference
- SPC-2008
- Primary DI / UDI-DI
- 10856602005144
- 510(k) Number
- FDA Product Code
- DXH, OZW
- GMDN Term
- Medication adherence telemetric monitoring system, post-ingestion
- Device Class
- Class II
- Regulation Number
- 870.2920, 880.6305
- Commercial Distribution
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Other devices from Proteus Digital Health, Inc.
Properties & raw data
Show properties, registry sources and raw records
Other properties (10)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Expiration Date: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 7a6f6486-013d-4f08-86aa-c7fc64866dcd