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Jedmed 03-6240

by JEDMED Instrument Company

Jedmed 03-6240 is an ENT cabinet (FDA Class I; FDA product code ETF, Unit, Examining/Treatment, Ent) made by JEDMED Instrument Company, listed in FDA GUDID since 3 Aug 2020 (UDI-DI M6330362400), 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 NumberM6330362400 UDI-DI Date3 Aug 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Jedmed
Generic name
ENT cabinet
Model / Ref / Catalog
03-6240
Primary DI / UDI-DI
M6330362400
FDA product code
ETF
GMDN term
ENT cabinet
Device class
Class I
Regulation number
874.5300
GUDID distribution status
In Commercial Distribution

Related devices

Category: ENT cabinet

Similar devices

Other devices filed under FDA product code ETF (Unit, Examining/Treatment, Ent).

Other devices from JEDMED Instrument Company

See all devices from JEDMED Instrument Company →

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)