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E9000 E9011-3

by Conmed Corporation

E9000 E9011-3 is a Class II device made by Conmed Corporation, listed in FDA GUDID since 24 Mar 2026 (UDI-DI 10845854035528), 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 Number10845854035528 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  • Withdrawn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
E9000
Generic name
Surgical instrument guard, reusable
Model / Ref / Catalog
E9011-3
Primary DI / UDI-DI
10845854035528
FDA product code
HRX
GMDN term
Surgical instrument guard, reusable
Device class
Class II
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)