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121205

by Tetra Medical Supply Corp.

121205 is a Class I device made by Tetra Medical Supply Corp., listed in FDA GUDID since 19 Aug 2022 (UDI-DI 00614138016071), 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 Number00614138016071 UDI-DI Date19 Aug 2022ListedStatusListed 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  • Withdrawn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

Generic name
Abdominal binder, reusable
Model / Ref / Catalog
121205
Primary DI / UDI-DI
00614138016071
FDA product code
FSD
GMDN term
Abdominal binder, reusable
Device class
Class I
Regulation number
880.5160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Abdominal binder, reusable

Similar devices in this category

Other devices filed under Abdominal binder, reusable.

Other devices from Tetra Medical Supply Corp.

See all devices from Tetra Medical Supply Corp. →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)