← Back to catalogue

β- HCG Assay Kit (Fluorescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref DL248001Model 20Tests/Kit

by DiYaLab ZJG Biotech Co., Ltd

Identity

Trade Name
β- HCG Assay Kit (Fluorescence Immunoassay) EUDAMED
Device Name
β- HCG Assay Kit (Fluorescence Immunoassay) EUDAMED
Model / Reference
20Tests/Kit EUDAMED
DL248001 EUDAMED

Identifiers

Primary DI / UDI-DI
06975424223455 EUDAMED
Basic UDI-DI
B-06975424223455 EUDAMED
EMDN Code
W0102050213 FREE BETA HCG (PRENATAL SCREENING) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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 Assay Kit (Fluorescence Immunoassay) by DiYaLab ZJG Biotech 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

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

Manufacturer

EUDAMED SRN
CN-MF-000048648
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED f4057f4f-36f9-467a-8ab8-1dc6c8c4574d 61 fields · synced Jul 14, 2026