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Zimmer Group

EUDAMED

Class I (EU MDR)

Ref LP1117-152-22F

by ZMI Electronics Ltd.

Identity

Trade Name
Zimmer Group EUDAMED
Device Name
Rubber Electrode EUDAMED
Model / Reference
LP1117-152-22F EUDAMED

Identifiers

Primary DI / UDI-DI
04719872331070 EUDAMED
Basic UDI-DI
471987233LPYV EUDAMED
EMDN Code
Z12062880 NEUROMUSCULAR STIMULATION EQUIPMENT - HARDWARE ACCESSORIES 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

Zimmer Group 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 07568fab-88dc-41c7-931e-004166d71d05 61 fields · synced Jun 19, 2026