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CoMoveIT Smart H2

EUDAMED

Class I (EU MDR)

Ref CM0001

by CoMoveIT

Identity

Trade Name
CoMoveIT Smart H2 EUDAMED
Device Name
CoMoveIT Smart EUDAMED
Model / Reference
CM0001 EUDAMED

Identifiers

Primary DI / UDI-DI
05430002911021 EUDAMED
Basic UDI-DI
5430002911CMSMART1DX EUDAMED
Direct Marketing DI
05430002911021 EUDAMED
EMDN Code
Y122403 WHEELCHAIR FOOTRESTS, SUPPORTS AND CONTROLS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

CoMoveIT Smart H2 by Comoveit — 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

Manufacturer
CoMoveIT
EUDAMED SRN
BE-MF-000017867

Sources (1)

  • EUDAMED 89fc0773-854d-42cc-b9a2-5d2b82dd53b2 61 fields · synced Jun 18, 2026