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Fibrinogen Detection Kit (Coagulation Assay)

EUDAMED

Class IVD General (EU MDR)

Ref R: 10×2.2mL; FIB Buffer: 1×51mL; FIB Reconstitution Fluid: 1×30mL; Calibrator: 1×1mL

by Dirui Industrial Co., Ltd

Identity

Device Name
Fibrinogen Detection Kit (Coagulation Assay) EUDAMED
Model / Reference
R: 10×2.2mL; FIB Buffer: 1×51mL; FIB Reconstitution Fluid: 1×30mL; Calibrator: 1×1mL EUDAMED

Identifiers

Primary DI / UDI-DI
06925794574671 EUDAMED
Basic UDI-DI
B-06925794574671 EUDAMED
EMDN Code
W0103020201 FIBRINOGEN ASSAYS (FACTOR I) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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

Fibrinogen Detection Kit (Coagulation Assay) by Dirui Industrial 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-000001891
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (3)

  • EUDAMED 416e6b53-e30b-4512-bc0c-ba2263b4c92d 61 fields · synced Jun 19, 2026
  • EUDAMED 416e6b53-e30b-4512-bc0c-ba2263b4c92d-1 61 fields · synced Jun 10, 2026
  • EUDAMED 416e6b53-e30b-4512-bc0c-ba2263b4c92d-2 61 fields · synced Jun 10, 2026