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PowerChek™ STI Multiplex Real-time PCR Kit Ⅲ

EUDAMED

Class IVD General (EU MDR)

Ref CQ19TTO0003Z

by KogeneBiotech Co., Ltd.

Identity

Trade Name
PowerChek™ STI Multiplex Real-time PCR Kit Ⅲ EUDAMED
Device Name
PowerChek™ STI Multiplex Real-time PCR Kit Ⅲ EUDAMED
Model / Reference
CQ19TTO0003Z EUDAMED

Identifiers

Primary DI / UDI-DI
08800056319024 EUDAMED
Basic UDI-DI
B-08800056319024 EUDAMED
EMDN Code
W0105070501 STIS / STDS (C.TRACHOMATIS, N.GONORRHOEAE ,M.GENITALIUM, T.VAGINALIS, UREAPLASMA SPP….) COMBINATION - MULTIPLEX NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

PowerChek™ STI Multiplex Real-time PCR Kit Ⅲ by KogeneBiotech 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
KR-MF-000045858
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 538075dd-affc-4f00-867d-3716056a0ca8 61 fields · synced Jun 19, 2026