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24K

by Conmed Corporation 3 variants

Ref D4024

24K (D4024) is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 6 Feb 2026 (Basic UDI-DI 084585408493DR) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20845854016494), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408493DR Basic UDI-DI 20845854016494UDI-DIDate6 Feb 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20845854016494 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408493DR registered 6 Feb 2026 Active
  • FDA GUDID UDI-DI 20845854016494 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 20845854016494
  2. Registered EUDAMED 084585408493DR

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  • Withdrawn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

Generic name
Electrical-only medical device connection cable, reusable
Device name
Orthopedic, Non-active, Accessory, Cable
Model / Ref / Catalog
D4024
Primary DI / UDI-DI
20845854016494
Basic UDI-DI
084585408493DR
Direct marketing DI
30845854016491
FDA product code
ERL, HBC, GEY
EMDN code
L0317 General surgery adapters and connectors, reusable
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
874.4250, 882.4360, 878.4820
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Length — 2 Meter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under GENERAL SURGERY ADAPTERS AND CONNECTORS, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)