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BioCLIA Autoimmune Reagent Kit, Jo-1

EUDAMED

Class IVD General (EU MDR)

Ref MY00102CModel Jo-1, 50 Tests/KitRef MY00153Model Jo-1, 100 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Autoimmune Reagent Kit, Jo-1 EUDAMED
Device Name
BioCLIA Autoimmune Reagent Kit, Jo-1 EUDAMED
Model / Reference
Jo-1, 50 Tests/Kit EUDAMED
MY00102C EUDAMED
Jo-1, 100 Tests/Kit EUDAMED
MY00153 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030415518 EUDAMED
06924030402686 EUDAMED
Basic UDI-DI
B-06924030415518 EUDAMED
B-06924030402686 EUDAMED
EMDN Code
W0102100108 JO-1 EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMEDEUDAMED

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, Jo-1 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 (2)

  • EUDAMED c69ce6cd-1bab-4639-ba1b-c709af832f77 61 fields · synced Jul 21, 2026
  • EUDAMED e68499f4-dd6a-4868-aad0-fb7b557a3f9f 61 fields · synced May 18, 2026