← Back to catalogue

CBC Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref HE50101

by Zhejiang Pushkang Biotechnology Co., Ltd.

Identity

Trade Name
CBC Assay Kit EUDAMED
Device Name
CBC Assay Kit EUDAMED
Model / Reference
HE50101 EUDAMED

Identifiers

Primary DI / UDI-DI
06975838800914 EUDAMED
Basic UDI-DI
B-06975838800914 EUDAMED
EMDN Code
W0103010103 COMPLETE CELL COUNT 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

CBC 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000042656
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED ed828cb3-b430-4087-9909-33c2339b0cfb 61 fields · synced Oct 6, 2026