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BioCLIA Autoimmune Reagent Kit, RF IgG

EUDAMED

Class IVD General (EU MDR)

Ref MY00129CModel RF IgG, 50 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Autoimmune Reagent Kit, RF IgG EUDAMED
Device Name
BioCLIA Autoimmune Reagent Kit, RF IgG EUDAMED
Model / Reference
RF IgG, 50 Tests/Kit EUDAMED
MY00129C EUDAMED

Identifiers

Primary DI / UDI-DI
06924030415785 EUDAMED
Basic UDI-DI
B-06924030415785 EUDAMED
EMDN Code
W01021110 RHEUMATOID FACTORS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

BioCLIA Autoimmune Reagent Kit, RF IgG by HOB Biotech Group Corp., 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-000023974
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 0d11e817-ee86-47c4-9799-746de6be6000 61 fields · synced Jul 22, 2026