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Neptune RT/XXL

EUDAMED

Class I (EU MDR)

Ref MR02230200809Model MR2230

by Mediroyal Nordic AB

Identity

Trade Name
Neptune RT/XXL EUDAMED
Device Name
Neptune EUDAMED
Model / Reference
MR2230 EUDAMED
MR02230200809 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032911954 EUDAMED
Basic UDI-DI
73400329MR22306E EUDAMED
Direct Marketing DI
07340032911954 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

Neptune RT/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 004c95a3-ed76-4b47-ac2d-3a2ab55d4a3b 61 fields · synced Jun 19, 2026