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Testing pack

EUDAMED

Class A (EU MDR)

Ref A060032Model 1 Tests/Kit

by Shenzhen Zijian Biotechnology Co., Ltd

Identity

Trade Name
Testing pack EUDAMED
Device Name
Testing pack EUDAMED
Model / Reference
1 Tests/Kit EUDAMED
A060032 EUDAMED

Identifiers

Primary DI / UDI-DI
06974674897003 EUDAMED
Basic UDI-DI
69746748900192A4 EUDAMED
EMDN Code
W0103010199 REAGENTS FOR (AUTOMATED) HAEMATOLOGY ANALYZER - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain 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

Testing pack by Shenzhen Zijian Biotechnology Co., Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000022829
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 78b24877-d113-4cda-b6bc-fb0d47fd0aa5 61 fields · synced Oct 5, 2026