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CEA/AFP Rapid Quantitative Test

EUDAMED

Class IVD General (EU MDR)

Ref BT2403

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
CEA/AFP Rapid Quantitative Test EUDAMED
Device Name
CEA/AFP Rapid Quantitative Test (Fluorescence Immunoassay) EUDAMED
Model / Reference
BT2403 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260208616 EUDAMED
Basic UDI-DI
B-06933260208616 EUDAMED
EMDN Code
W0102039099 TUMOUR MARKERS - OTHER 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

CEA/AFP Rapid Quantitative Test by Xiamen Biotime Biotechnology 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

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Manufacturer

EUDAMED SRN
CN-MF-000012852
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (2)

  • EUDAMED 758bb087-2c7c-4189-babc-f523d6b41b6e 61 fields · synced Jun 19, 2026
  • EUDAMED ebac9eea-4739-4ff5-9c0f-87c329b7ccc5 61 fields · synced Jun 19, 2026