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Electrical Stimulator PULSECURE Pro
EUDAMEDClass IIa (EU MDR)
Ref －Model KR-7002
Identity
- Trade Name
- Electrical Stimulator PULSECURE Pro EUDAMED
- Device Name
- Electrical Stimulator PULSECURE Pro EUDAMED
- Model / Reference
- KR-7002 EUDAMED－ EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04571292661713 EUDAMED
- Basic UDI-DI
- 45712926617133M EUDAMED
- EMDN Code
- Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED
Classification
- Device Class
- Class IIa 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
Electrical Stimulator PULSECURE Pro by OG Wellness Technologies Co., Ltd. Headquarters — Class IIa — 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 | 45712926617133M | Class IIa | Active |
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Manufacturer
- Manufacturer
- OG Wellness Technologies Co., Ltd. Headquarters
- EUDAMED SRN
- JP-MF-000002613
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED a1e50dc3-62d3-418c-9160-b276f1038bb7 61 fields · synced Jun 19, 2026