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Full Range C-Reactive Protein Test Kit (Latex-Enhanced Immunoturbidimetric Assa…

EUDAMED

Class C (EU MDR)

Ref /

by URIT Medical Electronic Co., Ltd.

Identity

Device Name
Full Range C-Reactive Protein Test Kit (Latex-Enhanced Immunoturbidimetric Assay) EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06935740713290 EUDAMED
Basic UDI-DI
69357407ICAS000025AW EUDAMED
EMDN Code
W01021109 C-REACTIVE PROTEIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

No

EUDAMED

Full Range C-Reactive Protein Test Kit (Latex-Enhanced Immunoturbidimetric Assa… by URIT Medical Electronic Co., Ltd. — Class C — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000011840
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED c4e8ffba-3065-4a7a-9582-e60b1926f8d2 61 fields · synced Jun 18, 2026