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Neptune Thumb Mid LT/XS

EUDAMED

Class I (EU MDR)

Ref MR02335100309Model MR2335

by Mediroyal Nordic AB

Identity

Trade Name
Neptune Thumb Mid LT/XS EUDAMED
Device Name
Neptune Thumb Mid EUDAMED
Model / Reference
MR2335 EUDAMED
MR02335100309 EUDAMED

Identifiers

Primary DI / UDI-DI
07340032913477 EUDAMED
Basic UDI-DI
73400329MR23356V EUDAMED
Direct Marketing DI
07340032913477 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 Thumb Mid 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 a06b4529-29cc-4987-abdc-55044ed50f4a 61 fields · synced Jun 18, 2026