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Kemilo hs-cTnI Kit

EUDAMED

Class IVD General (EU MDR)

Ref KM07060

by Goldsite Diagnostics Inc.

Identity

Trade Name
Kemilo hs-cTnI Kit EUDAMED
Device Name
Kemilo hs-cTnI Kit EUDAMED
Model / Reference
KM07060 EUDAMED

Identifiers

Primary DI / UDI-DI
06971225935818 EUDAMED
Basic UDI-DI
B-06971225935818 EUDAMED
EMDN Code
W01021306 TROPONIN I/T EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy 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

Kemilo hs-cTnI Kit by Goldsite Diagnostics Inc. — 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-000001353
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 553e3b63-94a1-4d65-b4b7-7be945d25a08 61 fields · synced Jul 8, 2026