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Conmed 136051

by Conmed Corporation

Part of a family of 11 devices: see the family page

Ref 136051

Conmed 136051 is an inert gas-enhanced electrosurgical system (EU MDR Class I; FDA Class II; FDA product code GEI, Electrosurgical, cutting & coagulation & accessories) made by Conmed Corporation, registered in EUDAMED on 11 Nov 2025 (Basic UDI-DI 084585408508DD), cleared under FDA 510(k) K050161 on 3 Feb 2005 and listed in FDA GUDID since 28 Apr 2020 (UDI-DI 10653405002987), active as of 23 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K050161

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408508DD Basic UDI-DI 10653405002987UDI-DIDate11 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405002987 UDI-DI Date28 Apr 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Special NumberK050161 Date3 Feb 2005DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 084585408508DD registered 11 Nov 2025 Active
  • FDA 510(k) K050161 decided 3 Feb 2005 Active
  • FDA GUDID UDI-DI 10653405002987 listed 28 Apr 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K050161
  2. Listed FDA GUDID 10653405002987
  3. Registered EUDAMED 084585408508DD

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Conmed
Generic name
Inert gas-enhanced electrosurgical system
Device name
Non-orthopedic, Non-active, Accessory, Cart/Cart attachment, General purpose
Model / Ref / Catalog
136051
Primary DI / UDI-DI
10653405002987
Basic UDI-DI
084585408508DD
510(k) Number
FDA product code
GEI
EMDN code
Z129099 Various instruments for functional exploration and therapeutic interventions - other
GMDN term
Inert gas-enhanced electrosurgical system
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: Inert gas-enhanced electrosurgical system

Similar devices

Also classified as Inert gas-enhanced electrosurgical system.

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - OTHER.

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)