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Nexstim Navigated Brain Therapy System

EUDAMED

Class IIa (EU MDR)

Ref NX88885

by Nexstim Oyj

Identity

Trade Name
Nexstim Navigated Brain Therapy System EUDAMED
Device Name
Nexstim Navigated Brain Therapy System EUDAMED
Model / Reference
NX88885 EUDAMED

Identifiers

Primary DI / UDI-DI
06430063200040 EUDAMED
Basic UDI-DI
B-06430063200040 EUDAMED
EMDN Code
Z12101106 NEUROLOGICAL STIMULATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Point aesthesiometer

Nexstim Navigated Brain Therapy System by Nexstim Oyj — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Point aesthesiometer.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Nexstim Oyj
EUDAMED SRN
FI-MF-000006696

Sources (1)

  • EUDAMED 5a20956e-d4f7-4b6b-95b7-9fd4a3785672 61 fields · synced Jul 18, 2026