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4-motion® knee tibial component

EUDAMED

Class III (EU MDR)

Ref 4631-L002

by ARTIQO GmbH

Identity

Trade Name
4-motion® knee tibial component EUDAMED
Device Name
4-motion® Tibia PSA zem., links Gr. 2 EUDAMED
Model / Reference
4631-L002 EUDAMED

Identifiers

Primary DI / UDI-DI
04251143404583 EUDAMED
Basic UDI-DI
B-04251143404583 EUDAMED
EMDN Code
P090903020104 BICOMPARTMENTAL PRIMARY IMPLANT CEMENTED FIXED BEARING TIBIAL PLATES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

4-motion® knee tibial component by ARTIQO GmbH — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
ARTIQO GmbH
EUDAMED SRN
DE-MF-000007336

Sources (1)

  • EUDAMED 43b1c598-b9f3-4578-b28f-a97d08f2295b 61 fields · synced Jun 18, 2026