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RF-IgM FIA Kit

EUDAMED

Class IVD General (EU MDR)

Ref 18-02-0051Model 25 Tests/kit

by Shenzhen Zijian Biotechnology Co., Ltd

Identity

Trade Name
RF-IgM FIA Kit EUDAMED
Device Name
RF-IgM FIA Kit EUDAMED
Model / Reference
25 Tests/kit EUDAMED
18-02-0051 EUDAMED

Identifiers

Primary DI / UDI-DI
06974674892213 EUDAMED
Basic UDI-DI
B-06974674892213 EUDAMED
EMDN Code
W01021110 RHEUMATOID FACTORS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

RF-IgM FIA Kit by Shenzhen Zijian 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-000022829
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED d0ff321e-93c6-44cc-8f2d-73d6a76a32c7 61 fields · synced Jun 20, 2026