40250228
by Wright Medical Technology, Inc.
Ref 40250228Model 08858251028081UC
40250228 is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 08858251028081UC) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00889797010733), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number08858251028081UC 00889797010733 | Date28 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889797010733 | Date17 Sep 2016 | StatusListed |
Official records
- EUDAMED public site 08858251028081UC
- AccessGUDID record 00889797010733
Across registries
- EUDAMED Basic UDI-DI 08858251028081UC registered 28 Oct 2026 Active
- FDA GUDID UDI-DI 00889797010733 listed 17 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00889797010733
- Registered EUDAMED 08858251028081UC
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Claw® II
- Generic name
- Surgical instrument guard, reusable
- Device name
- CLAW II Instrumentation - Instrumentation Sleeves - Class Ir - Reusable - Nonsterile
- Model / Ref / Catalog
- 40250228, 08858251028081UC
- Primary DI / UDI-DI
- 00889797010733
- Basic UDI-DI
- 08858251028081UC
- Direct marketing DI
- 00889797010733
- FDA product code
- MDM
- EMDN code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- GMDN term
- Surgical instrument guard, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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