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Dirui

EUDAMED

Class IVD General (EU MDR)

Ref 1×100 test/kit R1:1×4mL; R2:1×5mL; R3:1×5mL Calibrator High value:1×1mL; Calibrator Low value:1×1mL etc

by Dirui Industrial Co., Ltd

Identity

Trade Name
DIRUI EUDAMED
Device Name
Angiotensin II Detection Kit (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
1×100 test/kit R1:1×4mL; R2:1×5mL; R3:1×5mL Calibrator High value:1×1mL; Calibrator Low value:1×1mL etc EUDAMED

Identifiers

Primary DI / UDI-DI
06942202226434 EUDAMED
Basic UDI-DI
B-06942202226434 EUDAMED
EMDN Code
W0102060202 ANGIOTENSIN I / II 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
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED c6c8083b-f5ca-41fc-962a-3e7a3d92d6a0 61 fields · synced May 23, 2026