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BioCLIA Autoimmune Reagent Kit, Ro52

EUDAMED

Class IVD General (EU MDR)

Ref MY00155Model Ro52, 100 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Autoimmune Reagent Kit, Ro52 EUDAMED
Device Name
BioCLIA Autoimmune Reagent Kit, Ro52 EUDAMED
Model / Reference
Ro52, 100 Tests/Kit EUDAMED
MY00155 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030402709 EUDAMED
Basic UDI-DI
B-06924030402709 EUDAMED
EMDN Code
W0102100199 AUTOIMMUNE CONNECTIVE TISSUE DISEASES TESTING - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

BioCLIA Autoimmune Reagent Kit, Ro52 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 aedd6c1e-1d4a-4663-8cc4-e86657cdb9a1 61 fields · synced Aug 2, 2026