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Jedmed 70-5937

by JEDMED Instrument Company

Jedmed 70-5937 is a Class I device made by JEDMED Instrument Company, listed in FDA GUDID since 7 Feb 2023 (UDI-DI M6337059370), 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 NumberM6337059370 UDI-DI Date7 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  • Withdrawn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
Endoscope video camera
Model / Ref / Catalog
70-5937
Primary DI / UDI-DI
M6337059370
FDA product code
FWD
GMDN term
Endoscope video camera
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscope video camera

Other devices from JEDMED Instrument Company

See all devices from JEDMED Instrument Company →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)