Jedmed 54-2982

by JEDMED Instrument Company

Jedmed 54-2982 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 19 Jan 2023 (UDI-DI M6335429820), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberM6335429820 UDI-DI	Date19 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Jedmed
Generic name: Surgical soft-tissue manipulation forceps, alligator, reusable
Model / Ref / Catalog: 54-2982

Primary DI / UDI-DI: M6335429820
FDA product code: KAE
GMDN term: Surgical soft-tissue manipulation forceps, alligator, reusable

Device class: Class I
Regulation number: 874.4420
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from JEDMED Instrument Company

Jedmed 42-8260-1

Class I
Jedmed 42-8240-2

Class I
Jedmed 30-1705 Gg

Class I
Jedmed 39-7405

Class II

See all devices from JEDMED Instrument Company →

Properties

Sterilise before use
Premarket exempt

Other properties (13, all answered No)