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Amd-Ritmed A1090

by AMD Medicom Inc

Amd-Ritmed A1090 is a Class I device made by AMD Medicom Inc, listed in FDA GUDID since 24 Nov 2021 (UDI-DI 20686864055178), 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 Number20686864055178 UDI-DI Date24 Nov 2021ListedStatusListed 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  • Withdrawn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
Basic pillowcase, single-use
Model / Ref / Catalog
A1090
Primary DI / UDI-DI
20686864055178
FDA product code
KME
GMDN term
Basic pillowcase, single-use
Device class
Class I
Regulation number
880.6060
GUDID distribution status
In Commercial Distribution
Size
Length — 30 Inch
Width — 21 Inch

Similar devices

Other devices filed under FDA product code KME (Bedding, Disposable, Medical).

Other devices from AMD Medicom Inc

See all devices from AMD Medicom Inc →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)