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Milvue Suite

by Milvue

Ref V2.1

Milvue Suite (V2.1) is a Class IIa device made by Milvue, registered in EUDAMED on 3 Jan 2024 (Basic UDI-DI 37700247740001MG), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37700247740001MG Basic UDI-DI 03770024774023UDI-DIDate3 Jan 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
V2.1
Primary DI / UDI-DI
03770024774023
Basic UDI-DI
37700247740001MG
Direct marketing DI
03770024774023
EMDN code
Z11030592 Radiology instruments - medical device software
Device class
Class IIa
Special device type
Software
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000009787

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Properties

  • Measuring function
Other properties (13, all answered No)