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Carcinoembryonic Antigen (CEA)/Alpha-Fetoprotein (AFP) Diagnostic Kit (TRFIA)

EUDAMED

Class IVD General (EU MDR)

Ref DR-CM-A019Model 96 tests/kit

by Darui Biotechnology Co., Ltd.

Identity

Device Name
Carcinoembryonic Antigen (CEA)/Alpha-Fetoprotein (AFP) Diagnostic Kit (TRFIA) EUDAMED
Model / Reference
96 tests/kit EUDAMED
DR-CM-A019 EUDAMED

Identifiers

Primary DI / UDI-DI
06974671100106 EUDAMED
Basic UDI-DI
B-06974671100106 EUDAMED
EMDN Code
W0102030199 CANCER ANTIGENS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy 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

Carcinoembryonic Antigen (CEA)/Alpha-Fetoprotein (AFP) 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 2d1c5916-f0f2-4818-900f-b7c3d3b9a599 61 fields · synced Jul 27, 2026