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Gemore

EUDAMED

Class I (EU MDR)

Ref FA5090Model FA5050

by Gemore Technology Co., Ltd.

Identity

Trade Name
GEMORE EUDAMED
Device Name
Electrodes EUDAMED
Model / Reference
FA5050 EUDAMED
FA5090 EUDAMED

Identifiers

Primary DI / UDI-DI
04712832960440 EUDAMED
Basic UDI-DI
471283296electrode6N EUDAMED
EMDN Code
N010201 TENS SYSTEM ELECTRODES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Gemore by Gemore Technology Co., 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-000019446
Authorised Representative
Luana Med. B.V. NL-AR-000002750

Sources (1)

  • EUDAMED ead3b8c6-1ac0-4b71-80e1-c5fb654f46be 61 fields · synced May 29, 2026