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Zika Virus Nucleic Acid Detection Kit (Fluorescence)

EUDAMED

Class IVD General (EU MDR)

Ref Fa023

by Kangsheng Information Technology (Hangzhou) Co. LTD

Identity

Device Name
Zika Virus Nucleic Acid Detection Kit (Fluorescence) EUDAMED
Model / Reference
Fa023 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697994388Fa023WD7F EUDAMED
Basic UDI-DI
B-697994388Fa023WD7F EUDAMED
EMDN Code
W0105040531 ZIKA VIRUS - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Zika Virus Nucleic Acid Detection Kit (Fluorescence) by Kangsheng Information Technology (Hangzhou) Co. LTD — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000053775
Authorised Representative
Crealkraft GmbH DE-AR-000049943

Sources (1)

  • EUDAMED a9ba55de-35c6-4c85-a532-aeb74dab27dd 61 fields · synced Jul 9, 2026