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Two Concave Stimulus Electrodes

EUDAMED

Class I (EU MDR)

Ref 9010-0008-01

by Mecta Llc

Identity

Device Name
Two Concave Stimulus Electrodes EUDAMED
Model / Reference
9010-0008-01 EUDAMED

Identifiers

Primary DI / UDI-DI
10850037993014 EUDAMED
Basic UDI-DI
10850037993014H9 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

Two Concave Stimulus Electrodes by Mecta Llc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/MDR

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Manufacturer

Manufacturer
Mecta Llc
EUDAMED SRN
US-MF-000019538
Authorised Representative
ICON (LR) Limited IE-AR-000006507

Sources (1)

  • EUDAMED 9783a862-fd86-458e-8a68-05c404c1d9f8 61 fields · synced Jul 19, 2026