Skip to content

E9000 E9015

by Conmed Corporation 2 variants

E9000 E9015 is a Class II device made by Conmed Corporation, listed in FDA GUDID since 24 Mar 2026 (UDI-DI 10845854035559), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number10845854035559 UDI-DI Date24 Mar 2026ListedStatusListed GUDID: not 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  • Withdrawn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
Bone/joint surgical power tool motorized handpiece/set, electric, reusable
Model / Ref / Catalog
E9015
Primary DI / UDI-DI
10845854035559
FDA product code
HRX
GMDN term
Bone/joint surgical power tool motorized handpiece/set, electric, reusable
Device class
Class II
Regulation number
888.1100
GUDID distribution status
Not 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)