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α1-fetoprotein AFP assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref 69543760F000015TModel 100 Tests

by Beijing Leadman Biochemistry Co., Ltd.

Identity

Trade Name
α1-fetoprotein AFP assay Kit EUDAMED
Device Name
α1-fetoprotein AFP assay Kit EUDAMED
Model / Reference
100 Tests EUDAMED
69543760F000015T EUDAMED

Identifiers

Primary DI / UDI-DI
06954376012331 EUDAMED
Basic UDI-DI
B-06954376012331 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

Yes

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

α1-fetoprotein AFP assay Kit by Beijing Leadman Biochemistry 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-000020150
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED be45a63b-fb0e-4048-84e6-2ee22c571eb9 61 fields · synced Oct 7, 2026