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Neatec Erix Three Neuro RT/XS

EUDAMED

Class I (EU MDR)

Ref NEA940-RT/XSModel NEA940

by Mediroyal Nordic AB

Identity

Trade Name
Neatec Erix Three Neuro RT/XS EUDAMED
Device Name
Neatec Erix Three Neuro EUDAMED
Model / Reference
NEA940 EUDAMED
NEA940-RT/XS EUDAMED

Identifiers

Primary DI / UDI-DI
07340032924855 EUDAMED
Basic UDI-DI
73400329NEA9406L EUDAMED
Direct Marketing DI
07340032924855 EUDAMED
EMDN Code
Y060621 SHOULDER 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

Neatec Erix Three Neuro RT/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 cadc281d-fea4-4b38-aec2-8c1ebee9fea5 61 fields · synced Jul 23, 2026