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AFP Rapid Quantitative Test (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref BT0505605

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
AFP Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Device Name
AFP Rapid Quantitative Test (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
BT0505605 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260207169 EUDAMED
Basic UDI-DI
B-06933260207169 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

AFP Rapid Quantitative Test (Chemiluminescence Immunoassay) by Xiamen Biotime Biotechnology Co., Ltd. — Class IVD General — CE/MDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000012852
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED d476cd40-e152-41e4-a224-ab61d593f05e 61 fields · synced Oct 7, 2026
  • EUDAMED d8beec90-981b-467d-b525-78da430c490f 61 fields · synced Jul 12, 2026