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Alpha-fetoprotein Quantitative Diagnostic Kit (TRFIA )

EUDAMED

Class IVD General (EU MDR)

Ref DR-CM-A001Model 96 tests/kit

by Darui Biotechnology Co., Ltd.

Identity

Device Name
Alpha-fetoprotein Quantitative Diagnostic Kit (TRFIA ) EUDAMED
Model / Reference
96 tests/kit EUDAMED
DR-CM-A001 EUDAMED

Identifiers

Primary DI / UDI-DI
06974671100014 EUDAMED
Basic UDI-DI
B-06974671100014 EUDAMED
EMDN Code
W0102039001 ALPHAFETOPROTEIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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

Alpha-fetoprotein Quantitative Diagnostic Kit (TRFIA ) by Darui 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-000030310
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 1ed1cb8f-1004-4cda-92c7-0105947c3d38 61 fields · synced Jun 19, 2026