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NeXus-Q32

EUDAMED

Class I (EU MDR)

Ref 70-0006-0003

by Mind Media Europe B.V.

Identity

Device Name
NeXus-Q32 EUDAMED
Model / Reference
70-0006-0003 EUDAMED

Identifiers

Primary DI / UDI-DI
08719481550394 EUDAMED
Basic UDI-DI
0871948155NXQ32BZ EUDAMED
Direct Marketing DI
08719481550394 EUDAMED
EMDN Code
Z12062499 BIOFEEDBACK INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

NeXus-Q32 by Mind Media Europe B.V. — 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

EUDAMED SRN
NL-MF-000001576

Sources (1)

  • EUDAMED 8dab9db0-012b-44af-9632-001f361b6135 61 fields · synced Jul 29, 2026