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VenoTrain soft S 21260715324333

by Bauerfeind GmbH & Co.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04057532531669 UDI-DI Date28 Jan 2023ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
VenoTrain soft S
Generic Name
Compression/pressure sock/stocking, single-use
Model / Reference
21260715324333
Primary DI / UDI-DI
04057532531669
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

Related devices

Category: Compression/pressure sock/stocking, single-use

Cleared under the same submission (K860826)

Show all (12)

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Properties

  • Single Use
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No