OsteoMed 337-2716-SP-05
Ref 337-2716-SP-05
OsteoMed 337-2716-SP-05 is a device classified as Class IIb in the EU and Class II in the US made by Osteomed Corp., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00845694084444) and listed in FDA GUDID since 7 Aug 2015 (UDI-DI 00845694084444), active as of 7 Nov 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-00845694084444 00845694084444 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00845694084444 | Date7 Aug 2015 | StatusListed |
Official records
- EUDAMED public site B-00845694084444
- AccessGUDID record 00845694084444
Across registries
- EUDAMED Basic UDI-DI B-00845694084444 registered 29 Oct 2026 Active
- FDA GUDID UDI-DI 00845694084444 listed 7 Aug 2015 Listed
Timeline
- Listed FDA GUDID 00845694084444
- Registered EUDAMED B-00845694084444
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Acumed EUDAMEDOsteoMed GUDID
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device name
- Screw
- Model / Ref / Catalog
- 337-2716-SP-05
- Primary DI / UDI-DI
- 00845694084444
- Basic UDI-DI
- B-00845694084444
- FDA product code
- HRS
- EMDN code
- P09120601 Cortical screws
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 888.3030
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Spain
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 16 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIb | Class II |
| Implantable | Yes | No |
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