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AFO Dorsal Splint RT/L

EUDAMED

Class I (EU MDR)

Ref MR05801200609Model MR5801

by Mediroyal Nordic AB

Identity

Trade Name
AFO Dorsal Splint RT/L EUDAMED
Device Name
AFO Dorsal Splint EUDAMED
Model / Reference
MR5801 EUDAMED
MR05801200609 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032935479 EUDAMED
Basic UDI-DI
73400329MR58017S EUDAMED
Direct Marketing DI
07340032935479 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT 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

Category: Ankle/foot orthosis

AFO Dorsal Splint RT/L by Mediroyal Nordic AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

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 db60188f-8846-4ca9-8f0b-c5daac167235 61 fields · synced Jul 25, 2026