Bahadir USA Y405.07A
Bahadir USA Y405.07A is a Class II device made by Bahadir USA LLC, cleared under FDA 510(k) K131407 on 12 Aug 2014 and listed in FDA GUDID since 31 Jul 2017 (UDI-DI 00859982006698), 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 | Number00859982006698 | Date31 Jul 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK131407 | Date12 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00859982006698
- FDA 510(k) database K131407
Across registries
- FDA 510(k) K131407 decided 12 Aug 2014 Active
- FDA GUDID UDI-DI 00859982006698 listed 31 Jul 2017 Listed
Timeline
- Cleared FDA 510(k) K131407
- Listed FDA GUDID 00859982006698
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bahadir USA
- Generic name
- Device sterilization/disinfection container, reusable
- Model / reference
- Y405.07A
- Description
- MINI BOTTOM NON PERFORATED 300X140X70MM
- Primary DI / UDI-DI
- 00859982006698
- 510(k) Number
- FDA product code
- KCT
- GMDN term
- Device sterilization/disinfection container, reusable
- Device class
- Class II
- Regulation number
- 880.6850
- GUDID distribution status
- In Commercial Distribution
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