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VenoTrain delight 20662041224009

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 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046445903618 UDI-DI Date6 Oct 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 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  • Withdrawn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 delight
Generic Name
Compression/pressure sock/stocking, single-use
Model / Reference
20662041224009
Primary DI / UDI-DI
04046445903618
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)

Other devices from Bauerfeind GmbH & Co.

See all devices from Bauerfeind GmbH & Co. →

Properties

  • Single Use
  • Serial Number

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No