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Ventus Beige LT/XS

EUDAMED

Class I (EU MDR)

Ref MR02223100303Model MR2223

by Mediroyal Nordic AB

Identity

Trade Name
Ventus Beige LT/XS EUDAMED
Device Name
Ventus Beige EUDAMED
Model / Reference
MR2223 EUDAMED
MR02223100303 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032911411 EUDAMED
Basic UDI-DI
73400329MR22236H EUDAMED
Direct Marketing DI
07340032911411 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

Ventus Beige LT/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 1cb6e907-4dd2-4685-9315-054186f38715 61 fields · synced Jun 17, 2026