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Jedmed 99-8074

by JEDMED Instrument Company

Jedmed 99-8074 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 3 Feb 2023 (UDI-DI M6339980740), 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 NumberM6339980740 UDI-DI Date3 Feb 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  • Withdrawn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
Fibreoptic light cable, reusable
Model / Ref / Catalog
99-8074
Primary DI / UDI-DI
M6339980740
FDA product code
EQH
GMDN term
Fibreoptic light cable, reusable
Device class
Class I
Regulation number
874.4350
GUDID distribution status
In Commercial Distribution

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Properties

  • Premarket exempt
Other properties (14, all answered No)