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Amd-Ritmed A306

by AMD Medicom Inc

Amd-Ritmed A306 is a Class I device made by AMD Medicom Inc, listed in FDA GUDID since 13 Jan 2019 (UDI-DI 10686864050787), 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 Number10686864050787 UDI-DI Date13 Jan 2019ListedStatusListed 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  • Withdrawn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
Pressure bandage, non-latex, single-use
Model / Ref / Catalog
A306
Primary DI / UDI-DI
10686864050787
FDA product code
MHW
GMDN term
Pressure bandage, non-latex, single-use
Device class
Class I
Regulation number
880.5075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pressure bandage, non-latex, single-use

Similar devices

Other devices filed under FDA product code MHW (DRESSING, COMPRESSION).

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)