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24K

by Conmed Corporation 3 variants

Ref 24K900

24K (24K900) is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 12 Nov 2025 (Basic UDI-DI 084585408585DX) and listed in FDA GUDID since 27 Nov 2023 (UDI-DI 10845854041178), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408585DX Basic UDI-DI 10845854041178UDI-DIDate12 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854041178 UDI-DI Date27 Nov 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408585DX registered 12 Nov 2025 Active
  • FDA GUDID UDI-DI 10845854041178 listed 27 Nov 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854041178
  2. Registered EUDAMED 084585408585DX

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  • Withdrawn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, Remote/Hand Control
Model / Ref / Catalog
24K900
Primary DI / UDI-DI
10845854041178
Basic UDI-DI
084585408585DX
Direct marketing DI
30845854041172
FDA product code
HRX
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
888.1100
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

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
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)