2250-12-000
Ref 2250-12-000
2250-12-000 (225012000) is a Class I device made by Depuy (Ireland), registered in EUDAMED on 13 May 2026 (Basic UDI-DI 0603295a0003385) and listed in FDA GUDID since 24 Sep 2018 (UDI-DI 10603295108283), active as of 23 Oct 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 | Number0603295a0003385 10603295108283 | Date13 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10603295108283 | Date24 Sep 2018 | StatusListed |
Official records
- EUDAMED public site 0603295a0003385
- AccessGUDID record 10603295108283
Across registries
- EUDAMED Basic UDI-DI 0603295a0003385 registered 13 May 2026 Active
- FDA GUDID UDI-DI 10603295108283 listed 24 Sep 2018 Listed
Timeline
- Listed FDA GUDID 10603295108283
- Registered EUDAMED 0603295a0003385
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Surgical mallet
- Device name
- Mallet/Hammer
- Model / Ref / Catalog
- 2250-12-000, 225012000
- Primary DI / UDI-DI
- 10603295108283
- Basic UDI-DI
- 0603295a0003385
- Direct marketing DI
- 10603295108283
- FDA product code
- GFJ
- EMDN code
- L0903 Orthopaedic surgery hammers, reusable
- GMDN term
- Surgical mallet
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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