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Dex® Rt/Xs

EUDAMED

Class I (EU MDR)

Ref MR02270200309Model MR2270

by Mediroyal Nordic AB

Identity

Trade Name
DEX® RT/XS EUDAMED
Device Name
DEX® EUDAMED
Model / Reference
MR2270 EUDAMED
MR02270200309 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032932003 EUDAMED
Basic UDI-DI
73400329MR22706S EUDAMED
Direct Marketing DI
07340032932003 EUDAMED
EMDN Code
Y060606 HAND 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

Dex® Rt/Xs 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 a1f264fb-706e-4028-ae67-ec48d7a5c1c4 61 fields · synced Oct 6, 2026