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Sigma Patient Stimulus Cable

EUDAMED

Class I (EU MDR)

Ref 9438-0173Model SigmaStim Sigma 200J

by SigmaStim Domestic LLC

Identity

Device Name
Sigma Patient Stimulus Cable EUDAMED
Model / Reference
SigmaStim Sigma 200J EUDAMED
9438-0173 EUDAMED

Identifiers

Primary DI / UDI-DI
00850045508098 EUDAMED
Basic UDI-DI
00850045508098CT EUDAMED
EMDN Code
Z12109002 ELECTROCONVULSIVE THERAPY (ECT) EQUIPMENT EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Sigma Patient Stimulus Cable by SigmaStim Domestic LLC — 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

EUDAMED SRN
US-MF-000029359
Authorised Representative
ICON (LR) Limited IE-AR-000006507

Sources (1)

  • EUDAMED 01e0b23c-42a3-45d6-a3c3-136821cb54d2 61 fields · synced Jun 20, 2026