Identity
- Trade Name
- Everyway EUDAMED
- Device Name
- Cutaneous Electrode Pad EUDAMED
- Model / Reference
- KF75D EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04719871185636 EUDAMED
- Basic UDI-DI
- 471987118-ELECTRODE-H5 EUDAMED
- Direct Marketing DI
- 04719871185636 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 471987118-ELECTRODE-H5 | Class I | Active |
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Manufacturer
- Manufacturer
- Everyway Medical Instrument Co., Ltd.
- EUDAMED SRN
- TW-MF-000009887
- Authorised Representative
- Luana Med. B.V. NL-AR-000002750
Sources (1)
- EUDAMED 9b3e3d65-c293-43d2-8137-f41d6f46bef7 61 fields · synced May 23, 2026