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Jedmed 54-5750

by JEDMED Instrument Company

Jedmed 54-5750 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 19 Jan 2023 (UDI-DI M6335457500), 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 NumberM6335457500 UDI-DI Date19 Jan 2023ListedStatusListed 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  • Withdrawn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 foreign body extraction forceps
Model / Ref / Catalog
54-5750
Primary DI / UDI-DI
M6335457500
FDA product code
KAE
GMDN term
ENT foreign body extraction forceps
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: ENT foreign body extraction forceps

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Other devices filed under ENT foreign body extraction forceps.

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Properties

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