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Medi PCS25U1

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 9 Nov 2026. What this means

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00636257188422 UDI-DI Date27 Oct 2026ListedStatusListed 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  • Withdrawn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
Intermittent venous compression system pump
Model / reference
PCS25U1
Primary DI / UDI-DI
00636257188422
FDA product code
JOW
GMDN term
Intermittent venous compression system pump
Device class
Class II
Regulation number
870.5800
GUDID distribution status
In Commercial Distribution

Other devices from Medi Manufacturing, Inc.

See all devices from Medi Manufacturing, Inc. →

Properties

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

Other properties (11)

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