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RADI FAST COVID-19 Detection Kit

EUDAMED

Class IVD General (EU MDR)

Ref RV008F

by KH Medical Co., Ltd.

Identity

Device Name
RADI FAST COVID-19 Detection Kit EUDAMED
Model / Reference
RV008F EUDAMED

Identifiers

Primary DI / UDI-DI
08800204300072 EUDAMED
Basic UDI-DI
B-08800204300072 EUDAMED
EMDN Code
W0105040599 VIROLOGY - NA REAGENTS - 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

RADI FAST COVID-19 Detection Kit by KH Medical 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-000017883
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 63d45333-a1e2-4c80-9816-6e80906014f3 61 fields · synced Jul 26, 2026