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FIB Fibrinogen Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref Ir086

by Kangsheng Information Technology (Hangzhou) Co. LTD

Identity

Device Name
FIB Fibrinogen Test Kit EUDAMED
Model / Reference
Ir086 EUDAMED

Identifiers

Primary DI / UDI-DI
D-697994388Ir0863YFR EUDAMED
Basic UDI-DI
B-697994388Ir0863YFR EUDAMED
EMDN Code
W0103020101 PROTHROMBIN TIME ( QUICK TEST ) 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

FIB Fibrinogen Test Kit by Kangsheng Information Technology (Hangzhou) 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-000053775
Authorised Representative
Crealkraft GmbH DE-AR-000049943

Sources (1)

  • EUDAMED b28b25bc-21c3-41e5-925b-1197964e8705 61 fields · synced Jul 9, 2026