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Fourier rehab

EUDAMED

Class IIa (EU MDR)

Ref M1A01GModel M1A01M、M1A01M

by Changsha Fourier Medical Technology Co., Ltd.

Identity

Trade Name
Fourier rehab EUDAMED
Device Name
Ankle joint rehabilitation Equipment(AnkletMotus) EUDAMED
Model / Reference
M1A01M、M1A01M EUDAMED
M1A01G EUDAMED

Identifiers

Primary DI / UDI-DI
06975010000033 EUDAMED
Basic UDI-DI
697501000M1AHX EUDAMED
Direct Marketing DI
06975010000033 EUDAMED
EMDN Code
Z120616 ELECTROMECHANICAL SYSTEMS FOR PHYSICAL THERAPY EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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

Fourier rehab by Changsha Fourier Medical Technology Co., Ltd. — 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

EUDAMED SRN
CN-MF-000018147
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 2bf2207c-032e-47af-8c96-e7477d66c5e3 61 fields · synced Jun 19, 2026