OsteoMed 354-1808
OsteoMed 354-1808 is a Class II device made by Osteomed Corp., listed in FDA GUDID since 14 Jun 2016 (UDI-DI 00845694092326), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00845694092326 | Date14 Jun 2016 | StatusListed |
Official records
- AccessGUDID record 00845694092326
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- OsteoMed
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Model / Ref / Catalog
- 354-1808
- Primary DI / UDI-DI
- 00845694092326
- FDA product code
- HWC
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 8 Millimeter
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