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Dorsum Flexi XXL

EUDAMED

Class I (EU MDR)

Ref MR04926000809Model MR4926

by Mediroyal Nordic AB

Identity

Trade Name
Dorsum Flexi XXL EUDAMED
Device Name
Dorsum Flexi EUDAMED
Model / Reference
MR4926 EUDAMED
MR04926000809 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032908312 EUDAMED
Basic UDI-DI
73400329MR492688 EUDAMED
Direct Marketing DI
07340032908312 EUDAMED
EMDN Code
Y060308 LUMBOSACRAL SPINE 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

Dorsum Flexi 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 e8a2ee79-e070-498e-b2fa-6b826adffd0d 61 fields · synced Jul 31, 2026