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MicroFrance®

by Integra MicroFrance 44 variants

Part of a family of 22 devices: see the family page

Ref MCM25-3

MicroFrance® (MCM25-3) is a Class I device made by Integra Microfrance, registered in EUDAMED on 10 Jul 2026 (Basic UDI-DI 038178B0053CSS3E), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number038178B0053CSS3E Basic UDI-DI 10381780107385UDI-DIDate10 Jul 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Case and Tray
Model / reference
MCM25-3
Primary DI / UDI-DI
10381780107385
Basic UDI-DI
038178B0053CSS3E
EMDN code
V0402 Clinical use trays and bowls
Device class
Class I
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
FR-MF-000011524

Similar devices in this category

Other devices filed under CLINICAL USE TRAYS AND BOWLS.

Other devices from Integra Microfrance

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Properties

  • Sterilise before use
Other properties (13, all answered No)