← Back to catalogue

β-HCG Rapid Quantitative Test (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref HR0502002

by Xiamen BioRay Biotechnology Co., Ltd.

Identity

Device Name
β-HCG Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
HR0502002 EUDAMED

Identifiers

Primary DI / UDI-DI
06977194141472 EUDAMED
Basic UDI-DI
B-06977194141472 EUDAMED
EMDN Code
W0102160302 HCG - RT & POC 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

β-HCG Rapid Quantitative Test (Chemiluminescence Immunoassay) by Xiamen BioRay Biotechnology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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

Manufacturer

EUDAMED SRN
CN-MF-000045502
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED f49f058a-7c6d-45d9-8949-dfde2e46a249 61 fields · synced Jun 18, 2026