← Back to catalogue

EEG Green Reference Lead

EUDAMED

Class I (EU MDR)

Ref 9013-0001-03

by SigmaStim Domestic LLC

Identity

Device Name
EEG Green Reference Lead EUDAMED
Model / Reference
9013-0001-03 EUDAMED

Identifiers

Primary DI / UDI-DI
10850045508200 EUDAMED
Basic UDI-DI
10850045508200D5 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 Green Reference Lead 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 16923101-4ece-4b13-a5ab-8187984db4ce 61 fields · synced Jul 11, 2026