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EEG/EEG Five-Lead Set

EUDAMED

Class I (EU MDR)

Ref 9010-0011-13

by SigmaStim Domestic LLC

Identity

Device Name
EEG/EEG Five-Lead Set EUDAMED
Model / Reference
9010-0011-13 EUDAMED

Identifiers

Primary DI / UDI-DI
10850045508231 EUDAMED
Basic UDI-DI
10850045508231DG 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

EEG/EEG Five-Lead Set 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 71e4c8df-8dcc-4f07-b556-e14c6bb61d2e 61 fields · synced Jul 9, 2026