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Neisseria gonorrhoeae Antigen Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref Ir019

by Kangsheng Information Technology (Hangzhou) Co. LTD

Identity

Device Name
Neisseria gonorrhoeae Antigen Test Kit EUDAMED
Model / Reference
Ir019 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697994388Ir0193HDM EUDAMED
Basic UDI-DI
B-697994388Ir0193HDM EUDAMED
EMDN Code
W0105090199 BACTERIOLOGY - RT & POC - OTHER 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

Neisseria gonorrhoeae Antigen Test 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 869d3306-62b9-42af-9e21-8c11c0c752c4 61 fields · synced Jul 24, 2026