Versajet™ II 66800475
by Smith & Nephew Medical, Ltd.
Versajet™ II 66800475 is a Class II device made by Smith & Nephew Medical, Ltd., cleared under FDA 510(k) K143115 on 15 Jul 2015 and listed in FDA GUDID since 31 Aug 2018 (UDI-DI 00040565125503), 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 | Number00040565125503 | Date31 Aug 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK143115 | Date15 Jul 2015 | StatusActive |
Official records
- AccessGUDID record 00040565125503
- FDA 510(k) database K143115
Across registries
- FDA 510(k) K143115 decided 15 Jul 2015 Active
- FDA GUDID UDI-DI 00040565125503 listed 31 Aug 2018 Listed
Timeline
- Cleared FDA 510(k) K143115
- Listed FDA GUDID 00040565125503
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Versajet™ II
- Generic name
- Electromechanical device/system transport trolley
- Model / Ref / Catalog
- 66800475
- Primary DI / UDI-DI
- 00040565125503
- 510(k) Number
- FDA product code
- FQH
- GMDN term
- Electromechanical device/system transport trolley
- Device class
- Class II
- Regulation number
- 880.5475
- GUDID distribution status
- In Commercial Distribution
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