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ComfoCable

EUDAMED

Class I (EU MDR)

Ref CCBL

by Sooma Oy

Identity

Trade Name
ComfoCable EUDAMED
Device Name
ComfoCable EUDAMED
Model / Reference
CCBL EUDAMED

Identifiers

Primary DI / UDI-DI
06430067180287 EUDAMED
Basic UDI-DI
6430067180008V6 EUDAMED
Direct Marketing DI
06430067180287 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

ComfoCable 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 66233fed-b11b-417b-b81c-54cfc006ba6a 61 fields · synced Jun 20, 2026