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MicroFrance® MCO781

by Integra Microfrance

Ref MCO781

MicroFrance® MCO781 is a Class I device made by Integra Microfrance, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI B-10381780110040) and listed in FDA GUDID since 12 Jan 2018 (UDI-DI 10381780110040), 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-10381780110040 Basic UDI-DI 10381780110040UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10381780110040 UDI-DI Date12 Jan 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10381780110040 registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 10381780110040 listed 12 Jan 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10381780110040
  2. Registered EUDAMED B-10381780110040

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  • Withdrawn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
Tympanostomy tube inserter, reusable
Device name
Forceps with positioning function
Model / Ref / Catalog
MCO781
Primary DI / UDI-DI
10381780110040
Basic UDI-DI
B-10381780110040
FDA product code
KAE
EMDN code
L149099, Q0399
GMDN term
Tympanostomy tube inserter, 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: Tympanostomy tube inserter, reusable

Similar devices in this category

Other devices filed under ENT INSTRUMENTS, REUSABLE - OTHER.

Other devices from Integra Microfrance

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Properties

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