Skip to content

Amd-Ritmed A6061-Tlf

by AMD Medicom Inc

Amd-Ritmed A6061-Tlf is a Class I device made by AMD Medicom Inc, listed in FDA GUDID since 13 Jan 2019 (UDI-DI 20686864051613), 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 Number20686864051613 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  • Withdrawn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
Non-adhesive device retention bandage
Model / Ref / Catalog
A6061-TLF
Primary DI / UDI-DI
20686864051613
FDA product code
FQM
GMDN term
Non-adhesive device retention bandage
Device class
Class I
Regulation number
880.5075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Non-adhesive device retention bandage

Similar devices

Other devices filed under FDA product code FQM (BANDAGE, ELASTIC).

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)