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4-motion® Instrumenten-Sieb

EUDAMED

Class I (EU MDR)

Ref 9210000

by ARTIQO GmbH

Identity

Trade Name
4-motion® Instrumenten-Sieb EUDAMED
Device Name
Klasse I Zubehör, nicht-invasive Instrumente des 4-motion® Kniesystems, wiederverwendbar EUDAMED
Model / Reference
9210000 EUDAMED

Identifiers

Primary DI / UDI-DI
04251143403142 EUDAMED
Basic UDI-DI
42511434012003BW EUDAMED
Direct Marketing DI
04251143403142 EUDAMED
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

4-motion® Instrumenten-Sieb by ARTIQO GmbH — 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
ARTIQO GmbH
EUDAMED SRN
DE-MF-000007336

Sources (1)

  • EUDAMED 4fe24228-6c0b-4853-9936-2aa4c0d268fe 61 fields · synced Jul 14, 2026