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Abc 139330

by Conmed Corporation

Ref 139330

Abc 139330 is a device classified as Class IIb in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 18 Jun 2026 (Basic UDI-DI B-10653405055259) and listed in FDA GUDID since 7 Jul 2017 (UDI-DI 10653405055259), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10653405055259 Basic UDI-DI 10653405055259UDI-DIDate18 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405055259 UDI-DI Date7 Jul 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10653405055259 registered 18 Jun 2026 Active
  • FDA GUDID UDI-DI 10653405055259 listed 7 Jul 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10653405055259
  2. Registered EUDAMED B-10653405055259

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Abc
Generic name
Open-surgery electrosurgical electrode, monopolar, single-use
Device name
Non-orthopedic, Active, Instrument, Electrosurgical, Argon Pencil
Model / Ref / Catalog
139330
Primary DI / UDI-DI
10653405055259
Basic UDI-DI
B-10653405055259
FDA product code
GEI
EMDN code
K0204010101 Argon gas open surgery electrodes, single-use
GMDN term
Open-surgery electrosurgical electrode, monopolar, single-use
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.4400
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

Device class is stated on each registry's own scale: Class IIb 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: Open-surgery electrosurgical electrode, monopolar, single-use

Similar devices in this category

Other devices filed under DEVICES FOR SURGERY WITH ARGON GAS GENERATOR, SINGLE-USE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Single use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)