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Milvue Suite

EUDAMED

Class IIa (EU MDR)

Ref V2.1

by Milvue

Identity

Trade Name
Milvue Suite EUDAMED
Device Name
Milvue Suite EUDAMED
Model / Reference
V2.1 EUDAMED

Identifiers

Primary DI / UDI-DI
03770024774023 EUDAMED
Basic UDI-DI
37700247740001MG EUDAMED
Direct Marketing DI
03770024774023 EUDAMED
EMDN Code
Z11030592 RADIOLOGY INSTRUMENTS - MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Milvue Suite by Milvue — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Milvue
EUDAMED SRN
FR-MF-000009787

Sources (1)

  • EUDAMED 004d8fc5-0de8-486d-82b1-f15b5eeb60af 61 fields · synced Jul 10, 2026