← Back to catalogue

Alkaline Phosphatase Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref A001Model 125T

by Zhejiang Pushkang Biotechnology Co., Ltd.

Identity

Device Name
Alkaline Phosphatase Assay Kit EUDAMED
Model / Reference
125T EUDAMED
A001 EUDAMED

Identifiers

Primary DI / UDI-DI
06975838801447 EUDAMED
Basic UDI-DI
B-06975838801447 EUDAMED
EMDN Code
W01010105 ALKALINE PHOSPHATASE - TOTAL 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

Alkaline Phosphatase 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
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED a5a73212-79f3-4c1d-9136-c7ea5e5f9457 61 fields · synced Jun 18, 2026