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Conmed 714

by Conmed Corporation

Ref 714

Conmed 714 is an open-surgery electrosurgical electrode (EU MDD Class IIb; FDA Class II; FDA product code GEI, Electrosurgical, cutting & coagulation & accessories) made by Conmed Corporation, registered in EUDAMED on 19 Jun 2026 (Basic UDI-DI B-40653405014370) and listed in FDA GUDID since 1 Sep 2020 (UDI-DI 40653405014370), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-40653405014370 Basic UDI-DI 40653405014370UDI-DIDate19 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number40653405014370 UDI-DI Date1 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-40653405014370 registered 19 Jun 2026 Active
  • FDA GUDID UDI-DI 40653405014370 listed 1 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 40653405014370
  2. Registered EUDAMED B-40653405014370

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  • Withdrawn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
Conmed
Generic name
Open-surgery electrosurgical electrode, monopolar, reusable
Device name
Non-orthopedic, Active, Instrument, Electrosurgical, Electrode, Hyfrecator, Reusable
Model / Ref / Catalog
714
Primary DI / UDI-DI
40653405014370
Basic UDI-DI
B-40653405014370
FDA product code
GEI
EMDN code
L180302 Endoscopic electrosurgery handpieces, reusable
GMDN term
Open-surgery electrosurgical electrode, monopolar, reusable
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
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 0.375 Inch

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, reusable

Similar devices in this category

Other devices filed under ENDOSCOPIC ELECTROSURGERY HANDPIECES, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)