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hCG Rapid Test Device

EUDAMED

Class IVD General (EU MDR)

Ref G071216T

by Hangzhou Realy Tech Co., Ltd.

Identity

Trade Name
hCG Rapid Test Device EUDAMED
Model / Reference
G071216T EUDAMED

Identifiers

Primary DI / UDI-DI
06971792053038 EUDAMED
Basic UDI-DI
B-06971792053038 EUDAMED
EMDN Code
W0102050205 TOTAL HUMAN CHORIONIC GONADOTROPIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

hCG Rapid Test Device by Hangzhou Realy Tech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000004716
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED fce6c370-1c00-4019-a992-7096456b8376 61 fields · synced Jun 19, 2026