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GeneProof Neisseria gonorrhoeae PCR Kit

EUDAMED

Class C (EU MDR)

Ref NG/GP/025

by GeneProof a.s.

Identity

Trade Name
GeneProof Neisseria gonorrhoeae PCR Kit EUDAMED
Device Name
GeneProof Neisseria gonorrhoeae PCR Kit EUDAMED
Model / Reference
NG/GP/025 EUDAMED

Identifiers

Primary DI / UDI-DI
08595696300371 EUDAMED
Basic UDI-DI
859569630025QH EUDAMED
EMDN Code
W0105010203 GONOCOCCAL DETECTION BY NA REAGENTS EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Czechia 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

New Device

No

EUDAMED

GeneProof Neisseria gonorrhoeae PCR Kit by GeneProof a.s. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
GeneProof a.s.
EUDAMED SRN
CZ-MF-000002370

Sources (1)

  • EUDAMED 632928b8-1e2b-484d-a90b-387abdf0e15c 61 fields · synced Oct 6, 2026