40253200
by Wright Medical Technology, Inc.
Ref 40253200Model 08858251028147UH
40253200 is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 08858251028147UH) and listed in FDA GUDID since 27 Dec 2023 (UDI-DI 00889797010795), 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 | Number08858251028147UH 00889797010795 | Date5 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00889797010795 | Date27 Dec 2023 | StatusListed |
Official records
- EUDAMED public site 08858251028147UH
- AccessGUDID record 00889797010795
Across registries
- EUDAMED Basic UDI-DI 08858251028147UH registered 5 Nov 2026 Active
- FDA GUDID UDI-DI 00889797010795 listed 27 Dec 2023 Listed
Timeline
- Listed FDA GUDID 00889797010795
- Registered EUDAMED 08858251028147UH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Claw® II
- Generic name
- Instrument tray, reusable
- Device name
- Claw II Instrumentation - Trays and Tray Accessories - Class I - Nonsterile
- Model / Ref / Catalog
- 40253200, 08858251028147UH
- Primary DI / UDI-DI
- 00889797010795
- Basic UDI-DI
- 08858251028147UH
- Direct marketing DI
- 00889797010795
- FDA product code
- LRP
- EMDN code
- L098099 Orthopaedic and traumatological surgery instruments, reusable - other accessories
- GMDN term
- Instrument tray, 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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