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Ezlink

by Conmed Corporation

Part of a family of 14 devices: see the family page

Ref EZLINK01

Ezlink (EZLINK01) is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 11 Nov 2025 (Basic UDI-DI 084585408507DB) and listed in FDA GUDID since 25 Jun 2020 (UDI-DI 30845854081277), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408507DB Basic UDI-DI 30845854081277UDI-DIDate11 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number30845854081277 UDI-DI Date25 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408507DB registered 11 Nov 2025 Active
  • FDA GUDID UDI-DI 30845854081277 listed 25 Jun 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 30845854081277
  2. Registered EUDAMED 084585408507DB

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  • Withdrawn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
Non-orthopedic, Non-active, Accessory, Cable/Cord
Model / Ref / Catalog
EZLINK01
Primary DI / UDI-DI
30845854081277
Basic UDI-DI
084585408507DB
FDA product code
FYD
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
878.5070
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
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)