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Mat Platform

EUDAMED

Class I (EU MDR)

Ref -Model GH-7000F

by OG Wellness Technologies Co., Ltd. Headquarters

Identity

Trade Name
Mat Platform EUDAMED
Device Name
Mat Platform EUDAMED
Model / Reference
GH-7000F EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
04571292661492 EUDAMED
Basic UDI-DI
45712926614923U EUDAMED
EMDN Code
Z12069099 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class I 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

Mat Platform by OG Wellness Technologies Co., Ltd. Headquarters — 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
JP-MF-000002613
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED a77828bd-4e19-4750-96c6-4456f483d08a 61 fields · synced Jun 11, 2026