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MicroFrance® MCO23

by Integra Microfrance

Ref MCO23

MicroFrance® MCO23 is a Class I device made by Integra Microfrance, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI B-10381780108252) and listed in FDA GUDID since 12 Jan 2018 (UDI-DI 10381780108252), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10381780108252 Basic UDI-DI 10381780108252UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780108252 UDI-DI Date12 Jan 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10381780108252 registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 10381780108252 listed 12 Jan 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780108252
  2. Registered EUDAMED B-10381780108252

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  • Withdrawn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
Surgical soft-tissue manipulation forceps, alligator, reusable
Device name
Forceps with prehension function
Model / Ref / Catalog
MCO23
Primary DI / UDI-DI
10381780108252
Basic UDI-DI
B-10381780108252
FDA product code
KAE
EMDN code
L99, Q0399
GMDN term
Surgical soft-tissue manipulation forceps, alligator, reusable
Device class
Class I
Regulation number
874.4420
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

Related devices

Category: Surgical soft-tissue manipulation forceps, alligator, reusable

Similar devices in this category

Other devices filed under ENT DEVICES - OTHER.

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)