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Conmed 130142

by Conmed Corporation

Ref 130142

Conmed 130142 is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 27 Oct 2025 (Basic UDI-DI 084585408509DF) and listed in FDA GUDID since 30 Nov 2023 (UDI-DI 20653405002106), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408509DF Basic UDI-DI 20653405002106UDI-DIDate27 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number20653405002106 UDI-DI Date30 Nov 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585408509DF registered 27 Oct 2025 Active
  • FDA GUDID UDI-DI 20653405002106 listed 30 Nov 2023 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 20653405002106
  2. Registered EUDAMED 084585408509DF

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  • Withdrawn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
Medical equipment/instrument drape, single-use
Device name
Non-orthopedic, Non-active, Accessory, Drape/Sheath/Cover, Footswitch
Model / Ref / Catalog
130142
Primary DI / UDI-DI
20653405002106
Basic UDI-DI
084585408509DF
Unit of use DI
00653405002102
FDA product code
HAM
EMDN code
T030102 Cover sheaths, instruments and equipments
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4400
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.

Related devices

Category: Medical equipment/instrument drape, single-use

Similar devices in this category

Other devices filed under COVER SHEATHS, INSTRUMENTS AND EQUIPMENTS.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)