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Medi 50W34

by Medi Manufacturing, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number00636257175699 UDI-DI Date4 Apr 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Medi
Generic name
Compression/pressure sock/stocking, single-use
Model / reference
50W34
Primary DI / UDI-DI
00636257175699
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

Other devices from Medi Manufacturing, Inc.

See all devices from Medi Manufacturing, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (10)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No