ClariFix CFX-2002
ClariFix CFX-2002 is a nitrous oxide gas cartridge (FDA Class II; FDA product code GEH, Unit, Cryosurgical, Accessories) made by Stryker Corp., listed in FDA GUDID since 1 Sep 2020 (UDI-DI 00850002250411), registry data as of 2 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850002250411 | Date1 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00850002250411
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ClariFix
- Generic name
- Nitrous oxide gas cartridge
- Model / Ref / Catalog
- CFX-2002
- Primary DI / UDI-DI
- 00850002250411
- FDA product code
- GEH
- GMDN term
- Nitrous oxide gas cartridge
- Device class
- Class II
- Regulation number
- 878.4350
- GUDID distribution status
- In Commercial Distribution
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