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Gonorrhoea Rapid Test Kit(Swab)

EUDAMED

Class IVD General (EU MDR)

Ref GON-6012

by Safecare Biotech (hangzhou) Co., Ltd.

Identity

Trade Name
Gonorrhoea Rapid Test Kit(Swab) EUDAMED
Device Name
Gonorrhoea Rapid Test Kit(Swab) EUDAMED
Model / Reference
GON-6012 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697424646GON000KDYH EUDAMED
Basic UDI-DI
B-697424646GON000KDYH 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

Yes

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

Gonorrhoea Rapid Test Kit(Swab) by Safecare Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000019109
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED 2a1cc2e2-40e7-4d3b-bdb1-3b8df61e9d70 61 fields · synced Jul 26, 2026