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Artemide

EUDAMED

Class I (EU MDR)

Ref 1314501Model RIABILITAZIONE ARTI

by FISIOTECH srl

Identity

Trade Name
ARTEMIDE EUDAMED
Device Name
POLTRONA ARTEMIDE EUDAMED
Model / Reference
RIABILITAZIONE ARTI EUDAMED
1314501 EUDAMED

Identifiers

Primary DI / UDI-DI
80505939427226 EUDAMED
Basic UDI-DI
8050593941314501F8 EUDAMED
Direct Marketing DI
80505939427226 EUDAMED
EMDN Code
Y0504 ARMS, TORSO AND LEGS RE-EDUCATION DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Artemide by FISIOTECH srl — 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
FISIOTECH srl
EUDAMED SRN
IT-MF-000028185

Sources (1)

  • EUDAMED 46560331-48f1-4514-b159-9f22f419e29f 61 fields · synced Jun 18, 2026