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MicroFrance® MCO240

by Integra Microfrance

Ref MCO240

MicroFrance® MCO240 is a Class I device made by Integra Microfrance, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI B-10381780108313) and listed in FDA GUDID since 12 Jan 2018 (UDI-DI 10381780108313), 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-10381780108313 Basic UDI-DI 10381780108313UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780108313 UDI-DI Date12 Jan 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10381780108313 registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 10381780108313 listed 12 Jan 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780108313
  2. Registered EUDAMED B-10381780108313

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  • Withdrawn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
ENT elevator
Device name
Microsurgery with elevating function
Model / Ref / Catalog
MCO240
Primary DI / UDI-DI
10381780108313
Basic UDI-DI
B-10381780108313
FDA product code
KAD
EMDN code
L149002, Q0399
GMDN term
ENT elevator
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: ENT elevator

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Other devices filed under ENT LEVERS, REUSABLE.

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Properties

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