Skip to content

AMD-Ritmed A4440US

by AMD Medicom Inc

AMD-Ritmed A4440US is a Class I device made by AMD Medicom Inc, listed in FDA GUDID since 27 May 2025 (UDI-DI 10686864061516), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10686864061516 UDI-DI Date27 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
A4440US
Primary DI / UDI-DI
10686864061516
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

Similar devices

Other devices filed under FDA product code NAC (Dressing, wound, hydrophilic).

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, all answered No)