← Back to catalogue

Neptune Long RT/XL

EUDAMED

Class I (EU MDR)

Ref MR02231200709Model MR2231

by Mediroyal Nordic AB

Identity

Trade Name
Neptune Long RT/XL EUDAMED
Device Name
Neptune Long EUDAMED
Model / Reference
MR2231 EUDAMED
MR02231200709 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032912081 EUDAMED
Basic UDI-DI
73400329MR22316G EUDAMED
Direct Marketing DI
07340032912081 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 Long RT/XL 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mediroyal Nordic AB
EUDAMED SRN
SE-MF-000007821

Sources (1)

  • EUDAMED 6730fdae-f61f-4173-b900-04c4aa374ed1 61 fields · synced Jul 22, 2026