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CRP Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref HE50102

by Zhejiang Pushkang Biotechnology Co., Ltd.

Identity

Trade Name
CRP Assay Kit EUDAMED
Device Name
CRP Assay Kit EUDAMED
Model / Reference
HE50102 EUDAMED

Identifiers

Primary DI / UDI-DI
06975838800952 EUDAMED
Basic UDI-DI
B-06975838800952 EUDAMED
EMDN Code
W0103010199 REAGENTS FOR (AUTOMATED) HAEMATOLOGY ANALYZER - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Czechia 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

CRP Assay Kit by Zhejiang Pushkang Biotechnology 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-000042656
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 59b1a6cf-5c67-4594-9c48-3f574e0a1ec9 61 fields · synced Jul 9, 2026