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Uric Acid Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref B005Model 125T

by Zhejiang Pushkang Biotechnology Co., Ltd.

Identity

Device Name
Uric Acid Assay Kit EUDAMED
Model / Reference
125T EUDAMED
B005 EUDAMED

Identifiers

Primary DI / UDI-DI
06975838801522 EUDAMED
Basic UDI-DI
B-06975838801522 EUDAMED
EMDN Code
W01010232 URIC ACID 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

Category: Uric acid IVD, reagent

Uric Acid Assay Kit by Zhejiang Pushkang Biotechnology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, reagent.

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 4c2c4409-c607-44d8-b925-5644cf3e9079 61 fields · synced Jun 19, 2026