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Jedmed 49-4930-M

by JEDMED Instrument Company

Jedmed 49-4930-M is a Class II device made by JEDMED Instrument Company, listed in FDA GUDID since 3 Feb 2023 (UDI-DI M633494930M0), 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 NumberM633494930M0 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  • Withdrawn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
Rigid optical sinoscope
Model / Ref / Catalog
49-4930-M
Primary DI / UDI-DI
M633494930M0
FDA product code
EOB
GMDN term
Rigid optical sinoscope
Device class
Class II
Regulation number
874.4760
GUDID distribution status
In Commercial Distribution
Sterilisation method
Liquid Chemical

Similar devices

Other devices filed under FDA product code EOB (Nasopharyngoscope (Flexible Or Rigid)).

Other devices from JEDMED Instrument Company

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Properties

  • Sterilise before use
  • Serial number
Other properties (13, all answered No)