Cofoe KFZXJ002
by Cofoe Medical Technology Co., Ltd
Cofoe KFZXJ002 is a Class I device made by Cofoe Medical Technology Co., Ltd, listed in FDA GUDID since 29 Jul 2024 (UDI-DI 06950715502617), registry data as of 22 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 | Number06950715502617 | Date29 Jul 2024 | StatusListed |
Official records
- AccessGUDID record 06950715502617
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Cofoe
- Generic name
- Walker tray
- Model / reference
- KFZXJ002
- Primary DI / UDI-DI
- 06950715502617
- FDA product code
- ITJ
- GMDN term
- Walker tray
- Device class
- Class I
- Regulation number
- 890.3825
- GUDID distribution status
- In Commercial Distribution
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