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Alpha-Fetoprotein assay (CLIA)

EUDAMED

Class IVD General (EU MDR)

Ref 7C01V1-B-EU, 7C01U1-B-EU, 7C01P1-B-EU

by Xiamen Boson Biotech Co., Ltd.

Identity

Trade Name
Alpha-Fetoprotein assay (CLIA) EUDAMED
Device Name
Alpha-Fetoprotein assay (CLIA) EUDAMED
Model / Reference
7C01V1-B-EU, 7C01U1-B-EU, 7C01P1-B-EU EUDAMED

Identifiers

Primary DI / UDI-DI
D-7C01DC EUDAMED
Basic UDI-DI
B-7C01DC EUDAMED
EMDN Code
W0102039001 ALPHAFETOPROTEIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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 assay (CLIA) by Xiamen Boson 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

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Manufacturer

EUDAMED SRN
CN-MF-000001096
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (2)

  • EUDAMED 6b450109-3619-4222-af87-b83b97f6e1fa 61 fields · synced Jun 17, 2026
  • EUDAMED 6b450109-3619-4222-af87-b83b97f6e1fa-1 61 fields · synced Jun 9, 2026