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C Reactive Protein Determination Kit (Fluorescence Immunochromatographic Assay)

EUDAMED

Class C (EU MDR)

Ref P15002Model 25 tests

by Beijing Diagreat Biotechnologies Co., Ltd.

Identity

Trade Name
C Reactive Protein Determination Kit (Fluorescence Immunochromatographic Assay) EUDAMED
Device Name
C Reactive Protein Determination Kit (Fluorescence Immunochromatographic Assay) EUDAMED
Model / Reference
25 tests EUDAMED
P15002 EUDAMED

Identifiers

Primary DI / UDI-DI
06975182500188 EUDAMED
Basic UDI-DI
697518250P150026A EUDAMED
Direct Marketing DI
06975182500188 EUDAMED
EMDN Code
W01021109 C-REACTIVE PROTEIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

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

New Device

Yes

EUDAMED

C Reactive Protein Determination Kit (Fluorescence Immunochromatographic Assay) by Beijing Diagreat Biotechnologies Co., Ltd. — Class C — IVDR — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000019511
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED e5e5f88c-b392-4d3c-b3b0-4f4b352be1c5 61 fields · synced Jun 18, 2026