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MicroFrance® CP605M

by Integra Microfrance

Ref CP605M

MicroFrance® CP605M is a device classified as Class IIb in the EU and Class II in the US made by Integra Microfrance, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI B-10381780099901) and listed in FDA GUDID since 20 Sep 2016 (UDI-DI 10381780099901), 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-10381780099901 Basic UDI-DI 10381780099901UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780099901 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10381780099901 registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 10381780099901 listed 20 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780099901
  2. Registered EUDAMED B-10381780099901

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  • Withdrawn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
MicroFrance®
Generic name
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
Model / Ref / Catalog
CP605M
Primary DI / UDI-DI
10381780099901
Basic UDI-DI
B-10381780099901
FDA product code
GEI
EMDN code
L180601 Open electrosurgery electrodes, reusable
GMDN term
Open-surgery electrosurgical handpiece/electrode, bipolar, 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 — 150 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

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 handpiece/electrode, bipolar, reusable

Similar devices in this category

Other devices filed under OPEN ELECTROSURGERY ELECTRODES, REUSABLE.

Other devices from Integra Microfrance

See all devices from Integra Microfrance →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)