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KL-6 Rapid Test (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref P232103

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
KL-6 Rapid Test (FIA) EUDAMED
Device Name
KL-6 Rapid Test (FIA) EUDAMED
Model / Reference
P232103 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698602778 EUDAMED
Basic UDI-DI
B-16972698602778 EUDAMED
EMDN Code
W01021299 ORGAN FUNCTION ASSAYS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain 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

KL-6 Rapid Test (FIA) by Hangzhou Genesis Biodetection and Biocontrol 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-000013495
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED d9d99de5-c383-492d-a946-450d118080b1 61 fields · synced Jun 18, 2026