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Rheumatoid Factor Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref G002Model 125T

by Zhejiang Pushkang Biotechnology Co., Ltd.

Identity

Device Name
Rheumatoid Factor Assay Kit EUDAMED
Model / Reference
125T EUDAMED
G002 EUDAMED

Identifiers

Primary DI / UDI-DI
06975838801836 EUDAMED
Basic UDI-DI
B-06975838801836 EUDAMED
EMDN Code
W01021110 RHEUMATOID FACTORS 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

Rheumatoid Factor 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 83c313ad-bc13-4b07-a5e9-f263f04786bb 61 fields · synced Sep 18, 2026