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Hyfrecator 7-900-230

by Conmed Corporation

Ref 7-900-230

Hyfrecator 7-900-230 is an electrosurgical system generator (EU MDD Class IIb; FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Conmed Corporation, registered in EUDAMED on 17 Jun 2026 (Basic UDI-DI B-20653405031618) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20653405031618), 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-20653405031618 Basic UDI-DI 20653405031618UDI-DIDate17 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20653405031618 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-20653405031618 registered 17 Jun 2026 Active
  • FDA GUDID UDI-DI 20653405031618 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 20653405031618
  2. Registered EUDAMED B-20653405031618

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  • Withdrawn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
Hyfrecator
Generic name
Electrosurgical system generator
Device name
Electrosurgical Generators
Model / Ref / Catalog
7-900-230
Primary DI / UDI-DI
20653405031618
Basic UDI-DI
B-20653405031618
FDA product code
GEI
EMDN code
Z12010902 Electrosurgical units (esu) for general use
GMDN term
Electrosurgical system generator
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

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: Electrosurgical system generator

Similar devices in this category

Other devices filed under ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Sterilise before use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)