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Jedmed 42-8240-2

by JEDMED Instrument Company

Jedmed 42-8240-2 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 1 Sep 2020 (UDI-DI M63342824020), 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 NumberM63342824020 UDI-DI Date1 Sep 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  • Withdrawn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
Surgical soft-tissue manipulation forceps, alligator, reusable
Model / Ref / Catalog
42-8240-2
Primary DI / UDI-DI
M63342824020
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

Related devices

Category: Surgical soft-tissue manipulation forceps, alligator, reusable

Similar devices in this category

Other devices filed under Surgical soft-tissue manipulation forceps, alligator, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)