VenoTrain impuls 20763024600221
VenoTrain impuls 20763024600221 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 29 Jan 2023 (UDI-DI 04057532541408), 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 | Number04057532541408 | Date29 Jan 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK860826 | Date18 Jun 1986 | StatusActive |
Official records
- AccessGUDID record 04057532541408
- FDA 510(k) database K860826
Across registries
- FDA 510(k) K860826 decided 18 Jun 1986 Active
- FDA GUDID UDI-DI 04057532541408 listed 29 Jan 2023 Listed
Timeline
- Cleared FDA 510(k) K860826
- Listed FDA GUDID 04057532541408
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- VenoTrain impuls
- Generic name
- Compression/pressure sock/stocking, single-use
- Model / reference
- 20763024600221
- Primary DI / UDI-DI
- 04057532541408
- 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