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BioMoov

EUDAMED

Class I (EU MDR)

Ref MEG018

by Electronique Du Mazet

Identity

Trade Name
BioMoov EUDAMED
Device Name
BioMoov EUDAMED
Model / Reference
MEG018 EUDAMED

Identifiers

Primary DI / UDI-DI
03701330200746 EUDAMED
Basic UDI-DI
137013302MEG018KP1YM EUDAMED
EMDN Code
Z12069080 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

BioMoov by Electronique Du Mazet — Class I — 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

EUDAMED SRN
FR-MF-000001805

Sources (1)

  • EUDAMED b794c216-167b-491a-9ea4-89c2f5163560 61 fields · synced Sep 18, 2026