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Conmed D8652

by Conmed Corporation

Part of a family of 12 devices: see the family page

Ref D8652

Conmed D8652 is a Class I device made by Conmed Corporation, registered in EUDAMED on 30 Apr 2026 (Basic UDI-DI 084585408435DB) and listed in FDA GUDID since 28 Apr 2020 (UDI-DI 10845854034927), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408435DB Basic UDI-DI 10845854034927UDI-DIDate30 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854034927 UDI-DI Date28 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408435DB registered 30 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854034927 listed 28 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854034927
  2. Registered EUDAMED 084585408435DB

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Conmed
Generic name
Orthopaedic implant driver
Device name
Orthopedic, Non-active, Reusable Surgical Instrument, Passing/Retrieval
Model / Ref / Catalog
D8652
Primary DI / UDI-DI
10845854034927
Basic UDI-DI
084585408435DB
Direct marketing DI
20845854034924
FDA product code
LXH
EMDN code
L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
GMDN term
Orthopaedic implant driver
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implant driver

Similar devices in this category

Other devices filed under INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)