YiFang YF-001
by Shenzhen YI Fang Blister Packaging Co., Ltd.
YiFang YF-001 is a Class II device made by Shenzhen YI Fang Blister Packaging Co., Ltd., cleared under FDA 510(k) K240023 on 1 Mar 2024 and listed in FDA GUDID since 30 Aug 2024 (UDI-DI 06977488690006), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06977488690006 | Date30 Aug 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK240023 | Date1 Mar 2024 | StatusActive |
Official records
- AccessGUDID record 06977488690006
- FDA 510(k) database K240023
Across registries
- FDA 510(k) K240023 decided 1 Mar 2024 Active
- FDA GUDID UDI-DI 06977488690006 listed 30 Aug 2024 Listed
Timeline
- Cleared FDA 510(k) K240023
- Listed FDA GUDID 06977488690006
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- YiFang
- Generic name
- Electronic thermometer probe cover
- Model / reference
- YF-001
- Primary DI / UDI-DI
- 06977488690006
- 510(k) Number
- FDA product code
- FLL
- GMDN term
- Electronic thermometer probe cover
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Electronic thermometer probe cover.