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Everyway

EUDAMED

Class I (EU MDR)

Ref SG110130

by Everyway Medical Instrument Co., Ltd.

Identity

Trade Name
Everyway EUDAMED
Device Name
Cutaneous Electrode Pad EUDAMED
Model / Reference
SG110130 EUDAMED

Identifiers

Primary DI / UDI-DI
04719871185797 EUDAMED
Basic UDI-DI
471987118-ELECTRODE-H5 EUDAMED
Direct Marketing DI
04719871185797 EUDAMED
EMDN Code
N010201 TENS SYSTEM ELECTRODES 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

Everyway by Everyway Medical Instrument 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-000009887
Authorised Representative
Luana Med. B.V. NL-AR-000002750

Sources (1)

  • EUDAMED 82f6c4c4-b635-45ac-b543-654ee1daaea5 61 fields · synced May 23, 2026