← Back to catalogue

Electrical Stimulator IVES

EUDAMED

Class IIa (EU MDR)

Ref -Model GD-612

by OG Wellness Technologies Co., Ltd. Headquarters

Identity

Trade Name
Electrical Stimulator IVES EUDAMED
Device Name
Electrical Stimulator IVES EUDAMED
Model / Reference
GD-612 EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
04571292660549 EUDAMED
Basic UDI-DI
B-04571292660549 EUDAMED
EMDN Code
Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Electrical Stimulator IVES by OG Wellness Technologies Co., Ltd. Headquarters — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 26e91d30-0230-4419-ba32-d09f7117e758 61 fields · synced Jun 19, 2026