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Electrical Stimulator PHYSIOUS

EUDAMED

Class IIa (EU MDR)

Ref -Model FS-250

by OG Wellness Technologies Co., Ltd. Headquarters

Identity

Trade Name
Electrical Stimulator PHYSIOUS EUDAMED
Device Name
Electrical Stimulator PHYSIOUS EUDAMED
Model / Reference
FS-250 EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
04571292660556 EUDAMED
Basic UDI-DI
45712926605563N 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 PHYSIOUS 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

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Manufacturer

EUDAMED SRN
JP-MF-000002613
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 7924315e-6d5c-45a6-9cdd-65966f18ebf2 61 fields · synced Jul 16, 2026