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Dirui

EUDAMED

Class IVD General (EU MDR)

Ref 3009927Model R1: 1×10mL, R2: 1×10mL, Diluent: 1×55mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
DIRUI EUDAMED
Device Name
Fibrin (Fibrinogen) Degradation Products Detection Kit (Latex Immunoturbidimetric Assay) EUDAMED
Model / Reference
R1: 1×10mL, R2: 1×10mL, Diluent: 1×55mL EUDAMED
3009927 EUDAMED

Identifiers

Primary DI / UDI-DI
06925794574145 EUDAMED
Basic UDI-DI
B-06925794574145 EUDAMED
EMDN Code
W0103020502 FIBRINOGEN DEGRADATION PRODUCTS 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

Dirui 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
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED fd40bc60-ef96-4171-95c9-ba25c0fe66e2 61 fields · synced May 23, 2026