COMBI *M sensor 82 0605000
COMBI *M sensor 82 0605000 is a Class II device made by Radiometer Basel AG, listed in FDA GUDID since 1 Sep 2016 (UDI-DI 05700693095189), not in commercial distribution (GUDID) as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05700693095189 | Date1 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 05700693095189
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- COMBI *M sensor 82
- Generic name
- Transcutaneous blood gas monitor sensor
- Model / Ref / Catalog
- 0605000
- Primary DI / UDI-DI
- 05700693095189
- FDA product code
- KLK, LKD
- GMDN term
- Transcutaneous blood gas monitor sensor
- Device class
- Class II
- Regulation number
- 868.2500, 868.2480
- GUDID distribution status
- Not in Commercial Distribution
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