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Salmonella typhi/paratyphi Nucleic Acid Detection Kit

EUDAMED

Class IVD General (EU MDR)

Ref Nc012

by Kangsheng Information Technology (Hangzhou) Co. LTD

Identity

Device Name
Salmonella typhi/paratyphi Nucleic Acid Detection Kit EUDAMED
Model / Reference
Nc012 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697994388Nc012ZECG EUDAMED
Basic UDI-DI
B-697994388Nc012ZECG EUDAMED
EMDN Code
W0105011001 SALMONELLA ANTIGEN DETECTION 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

Salmonella typhi/paratyphi Nucleic Acid Detection Kit 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 667be09f-6efb-4b5f-bdf8-34701bf1ba9b 61 fields · synced Jul 15, 2026