SemiFlex Scope MF-ENDO 60 E
SemiFlex Scope MF-ENDO 60 E is a Class II device made by Maxiflex, LLC, cleared under FDA 510(k) K111480 on 4 Apr 2012 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI B324MFENDO60E0), 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 | NumberB324MFENDO60E0 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK111480 | Date4 Apr 2012 | StatusActive |
Official records
- FDA 510(k) database K111480
Across registries
- FDA 510(k) K111480 decided 4 Apr 2012 Active
- FDA GUDID UDI-DI B324MFENDO60E0 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K111480
- Listed FDA GUDID B324MFENDO60E0
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- SemiFlex Scope
- Generic name
- Flexible fibreoptic ureteroscope
- Model / reference
- MF-ENDO 60 E
- Primary DI / UDI-DI
- B324MFENDO60E0
- 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
- Hydrogen Peroxide
- Size
- Catheter Gauge — 9.5 FrenchLength — 60 Centimeter
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