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Dirui

EUDAMED

Class IVD General (EU MDR)

Ref R1:1×45mL R2:1×15mL Calibrator :4×0.5mL Control :2×0.5mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
DIRUI EUDAMED
Device Name
Ceruloplasmin Reagent Kit (Immunoturbidimetric Assay) EUDAMED
Model / Reference
R1:1×45mL R2:1×15mL Calibrator :4×0.5mL Control :2×0.5mL EUDAMED

Identifiers

Primary DI / UDI-DI
06942202229169 EUDAMED
Basic UDI-DI
B-06942202229169 EUDAMED
EMDN Code
W0102010301 CERULOPLASMIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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 e3880867-f307-4cbe-92bf-3e01b4313360 61 fields · synced May 23, 2026