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Sodium Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref L002Model 80T

by Zhejiang Pushkang Biotechnology Co., Ltd.

Identity

Device Name
Sodium Assay Kit EUDAMED
Model / Reference
80T EUDAMED
L002 EUDAMED

Identifiers

Primary DI / UDI-DI
06975838801812 EUDAMED
Basic UDI-DI
B-06975838801812 EUDAMED
EMDN Code
W01010309 SODIUM EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy 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

Sodium 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
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED 516945e4-c145-4fde-ba8a-cc3adb2fb2a9 61 fields · synced Aug 2, 2026