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Tech-Med 4348

by Dukal LLC

Tech-Med 4348 is a Class I device made by Dukal LLC, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 20665973022202), 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 Number20665973022202 UDI-DI Date6 Dec 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  • Withdrawn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

Trade name
Tech-Med
Generic name
General-purpose stool/chair
Model / Ref / Catalog
4348
Primary DI / UDI-DI
20665973022202
FDA product code
FZM
GMDN term
General-purpose stool/chair
Device class
Class I
Regulation number
878.4950
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose stool/chair

Similar devices

Other devices filed under FDA product code FZM (STOOL, OPERATING-ROOM).

Other devices from Dukal LLC

See all devices from Dukal LLC →

Properties

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