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Finecare

EUDAMED

Class IVD General (EU MDR)

Ref W208

by Guangzhou Wondfo Biotech Co., Ltd.

Identity

Trade Name
Finecare EUDAMED
Device Name
FinecareTM AFP Rapid Quantitative Test EUDAMED
Model / Reference
W208 EUDAMED

Identifiers

Primary DI / UDI-DI
06933289810234 EUDAMED
Basic UDI-DI
B-06933289810234 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

Yes

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

Finecare by Guangzhou Wondfo 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-000000689
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 4ec92a72-93a3-4768-aa5e-05e3bbbb1d94 61 fields · synced Jun 18, 2026