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Amd-Ritmed A3340

by AMD Medicom 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 Number10686864050862 UDI-DI Date15 Jan 2019ListedStatusListed 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  • Withdrawn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
Amd-Ritmed
Generic name
Non-woven gauze pad
Model / Ref / Catalog
A3340
Primary DI / UDI-DI
10686864050862
FDA product code
NAC
GMDN term
Non-woven gauze pad
Device class
Class I
Regulation number
878.4018
GUDID distribution status
In Commercial Distribution

Related devices

Category: Non-woven gauze pad

Other devices from AMD Medicom Inc

See all devices from AMD Medicom Inc →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date

Other properties (9)

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