VenoTrain micro 21864714500332
VenoTrain micro 21864714500332 is a Class II device made by Bauerfeind GmbH & Co., cleared under FDA 510(k) K860826 on 18 Jun 1986 and listed in FDA GUDID since 18 Jan 2019 (UDI-DI 04046445308482), active as of 9 Nov 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 | Number04046445308482 | Date18 Jan 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK860826 | Date18 Jun 1986 | StatusActive |
Official records
- AccessGUDID record 04046445308482
- FDA 510(k) database K860826
Across registries
- FDA 510(k) K860826 decided 18 Jun 1986 Active
- FDA GUDID UDI-DI 04046445308482 listed 18 Jan 2019 Listed
Timeline
- Cleared FDA 510(k) K860826
- Listed FDA GUDID 04046445308482
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- VenoTrain micro
- Generic name
- Compression/pressure sock/stocking, single-use
- Model / reference
- 21864714500332
- Primary DI / UDI-DI
- 04046445308482
- 510(k) Number
- FDA product code
- DWL
- GMDN term
- Compression/pressure sock/stocking, single-use
- Device class
- Class II
- Regulation number
- 880.5780
- GUDID distribution status
- In Commercial Distribution