Container 256008
by Fournitures Hospitalieres Industrie
Container 256008 is a Class II device made by Fournitures Hospitalieres Industrie, cleared under FDA 510(k) K120740 on 5 Mar 2013 (1 earlier submission) and listed in FDA GUDID since 13 Mar 2019 (UDI-DI 03661489560088), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03661489560088 | Date13 Mar 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK120740 | Date5 Mar 2013 | StatusActive |
Official records
- AccessGUDID record 03661489560088
- FDA 510(k) database K120740
- FDA 510(k) database K113591
Across registries
- FDA 510(k) K120740 decided 5 Mar 2013 Active
- FDA GUDID UDI-DI 03661489560088 listed 13 Mar 2019 Listed
Timeline
- Cleared FDA 510(k) K113591
- Cleared FDA 510(k) K120740
- Listed FDA GUDID 03661489560088
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Container
- Generic name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / reference
- 256008
- Primary DI / UDI-DI
- 03661489560088
- FDA product code
- HWC, MBI
- GMDN term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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