← Back to catalogue

Finecare

EUDAMED

Class IVD Annex II List B (EU MDR)

Ref W209

by Guangzhou Wondfo Biotech Co., Ltd.

Identity

Trade Name
Finecare EUDAMED
Device Name
Finecare™ PSA Rapid Quantitative Test EUDAMED
Model / Reference
W209 EUDAMED

Identifiers

Primary DI / UDI-DI
06933289810241 EUDAMED
Basic UDI-DI
B-06933289810241 EUDAMED
EMDN Code
W0102030113 TOTAL PROSTATIC SPECIFIC ANTIGEN EUDAMED

Classification

Device Class
Class IVD Annex II List B 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 Annex II List B — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000000689
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 6167d318-2472-40b7-bc7d-54fbdbf50647 61 fields · synced Aug 1, 2026