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Sooma tDCS

EUDAMED

Class IIa (EU MDR)

Ref Sooma tDCS

by Sooma Oy

Identity

Trade Name
Sooma tDCS EUDAMED
Device Name
Sooma tDCS EUDAMED
Model / Reference
Sooma tDCS EUDAMED

Identifiers

Primary DI / UDI-DI
06430067180003 EUDAMED
Basic UDI-DI
B-06430067180003 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Point aesthesiometer

Sooma tDCS by Sooma Oy — 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
Sooma Oy
EUDAMED SRN
FI-MF-000004844

Sources (1)

  • EUDAMED b487a23e-827e-48cd-b1f1-835129619599 61 fields · synced Jul 27, 2026