Bagley REXMR-6A
Bagley REXMR-6A is a Class II device made by Gyrus Acmi, Inc., cleared under FDA 510(k) K052044 on 16 Aug 2005 and listed in FDA GUDID since 6 Oct 2016 (UDI-DI 00821925007826), active as of 23 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 | Number00821925007826 | Date6 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK052044 | Date16 Aug 2005 | StatusActive |
Official records
- AccessGUDID record 00821925007826
- FDA 510(k) database K052044
Across registries
- FDA 510(k) K052044 decided 16 Aug 2005 Active
- FDA GUDID UDI-DI 00821925007826 listed 6 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K052044
- Listed FDA GUDID 00821925007826
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Bagley
- Generic name
- Flexible fibreoptic ureteroscope
- Model / reference
- REXMR-6A
- Primary DI / UDI-DI
- 00821925007826
- 510(k) Number
- FDA product code
- FGB
- GMDN term
- Flexible fibreoptic ureteroscope
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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