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ARX® Patella Luxation Knee XXL

EUDAMED

Class I (EU MDR)

Ref ARX330-XXLModel ARX330

by Mediroyal Nordic AB

Identity

Trade Name
ARX® Patella Luxation Knee XXL EUDAMED
Device Name
ARX® Patella Luxation Knee EUDAMED
Model / Reference
ARX330 EUDAMED
ARX330-XXL EUDAMED

Identifiers

Primary DI / UDI-DI
07340032919981 EUDAMED
Basic UDI-DI
73400329ARX3309S EUDAMED
Direct Marketing DI
07340032919981 EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

ARX® Patella Luxation Knee XXL by Mediroyal Nordic AB — 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
Mediroyal Nordic AB
EUDAMED SRN
SE-MF-000007821

Sources (1)

  • EUDAMED 95825ead-dd8d-4c2c-881c-fe07fc31baab 61 fields · synced Jun 18, 2026