Identity
- Device Name
- NeXus-10 MKII EUDAMED
- Model / Reference
- 70-0002-0001, 70-0002-0002 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08719481550387 EUDAMED
- Basic UDI-DI
- 0871948155NX10MKII26 EUDAMED
- Direct Marketing DI
- 08719481550387 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-10 MKII 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0871948155NX10MKII26 | Class I | Active |
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Manufacturer
- Manufacturer
- Mind Media Europe B.V.
- EUDAMED SRN
- NL-MF-000001576
Sources (1)
- EUDAMED b30233f8-81d0-4e8b-99dc-3563f7ebf932 61 fields · synced Jun 9, 2026