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Bordetella pertussis Nucleic Acid Detection Kit (Fluorescence, Unvaccinated)

EUDAMED

Class IVD General (EU MDR)

Ref Fa038

by Kangsheng Information Technology (Hangzhou) Co. LTD

Identity

Device Name
Bordetella pertussis Nucleic Acid Detection Kit (Fluorescence, Unvaccinated) EUDAMED
Model / Reference
Fa038 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697994388Fa038WS9D EUDAMED
Basic UDI-DI
B-697994388Fa038WS9D EUDAMED
EMDN Code
W0105011607 BORDETELLA PERTUSSIS / PARAPERTUSSIS - 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

Bordetella pertussis Nucleic Acid Detection Kit (Fluorescence, Unvaccinated) by Kangsheng Information Technology (Hangzhou) Co. LTD — Class IVD General — IVDD…

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 32708751-6a8c-49d8-ae4d-dae4476a0492 61 fields · synced Jun 20, 2026