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ComfoTrode, CE25

EUDAMED

Class I (EU MDR)

Ref CE25

by Sooma Oy

Identity

Trade Name
ComfoTrode, CE25 EUDAMED
Device Name
ComfoTrode EUDAMED
Model / Reference
CE25 EUDAMED

Identifiers

Primary DI / UDI-DI
06430067180140 EUDAMED
Basic UDI-DI
6430067180003UU EUDAMED
EMDN Code
Z12101185 PERIPHERAL OR CENTRAL NEURO STIMULATION AND ASSESSMENT INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

ComfoTrode, CE25 by Sooma Oy — 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
Sooma Oy
EUDAMED SRN
FI-MF-000004844

Sources (1)

  • EUDAMED 04267afc-54f9-429a-81c5-7e123a5fa656 61 fields · synced Jun 18, 2026