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LH Rapid Quantitative Test (Fluorescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref HR0202601

by Xiamen BioRay Biotechnology Co., Ltd.

Identity

Device Name
LH Rapid Quantitative Test (Fluorescence Immunoassay) EUDAMED
Model / Reference
HR0202601 EUDAMED

Identifiers

Primary DI / UDI-DI
06977194141762 EUDAMED
Basic UDI-DI
B-06977194141762 EUDAMED
EMDN Code
W0102160304 LH - 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

LH Rapid Quantitative Test (Fluorescence 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

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Manufacturer

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

Sources (1)

  • EUDAMED 9925327a-6c17-4a7b-9198-a6b9c7104914 61 fields · synced Jun 18, 2026