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Rubber Electrode

EUDAMED

Class I (EU MDR)

Ref LP46-502-24M

by ZMI Electronics Ltd.

Identity

Device Name
Rubber Electrode EUDAMED
Model / Reference
LP46-502-24M EUDAMED

Identifiers

Primary DI / UDI-DI
04719872331216 EUDAMED
Basic UDI-DI
471987233LPYV EUDAMED
EMDN Code
Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Rubber Electrode by ZMI Electronics Ltd. — 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
TW-MF-000003571
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED c878f696-9551-47cd-b340-c5c023176147 61 fields · synced Jun 18, 2026