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ARX® Patella Luxation Knee S

EUDAMED

Class I (EU MDR)

Ref ARX330-SModel ARX330Ref ARX331-RT/SModel ARX331

by Mediroyal Nordic AB

Identity

Trade Name
ARX® Patella Luxation Knee S EUDAMED
ARX® Patella Luxation Long Knee RT/S EUDAMED
Device Name
ARX® Patella Luxation Knee EUDAMED
ARX® Patella Luxation Long Knee EUDAMED
Model / Reference
ARX330 EUDAMED
ARX330-S EUDAMED
ARX331 EUDAMED
ARX331-RT/S EUDAMED

Identifiers

Primary DI / UDI-DI
07340032919943 EUDAMED
07340032921861 EUDAMED
Basic UDI-DI
73400329ARX3309S EUDAMED
73400329ARX3319U EUDAMED
Direct Marketing DI
07340032919943 EUDAMED
07340032921861 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 S 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 (2)

  • EUDAMED 400fcb4a-4013-494d-b65b-2ee7e690ece6 61 fields · synced Oct 6, 2026
  • EUDAMED 259a602d-9f0c-45e1-9678-a1a17d93c86a 61 fields · synced May 17, 2026