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Conmed 000249

by Conmed Corporation 2 variants

Conmed 000249 is a Class II device made by Conmed Corporation, listed in FDA GUDID since 24 Mar 2026 (UDI-DI 10653405050865), 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 Number10653405050865 UDI-DI Date24 Mar 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Conmed
Generic name
Instrument tray, reusable
Model / Ref / Catalog
000249
Primary DI / UDI-DI
10653405050865
FDA product code
KNQ
GMDN term
Instrument tray, reusable
Device class
Class II
Regulation number
876.5365
GUDID distribution status
In Commercial Distribution

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)