← Back to catalogue

BioCLIA Autoimmune Reagent Kit, IA2

EUDAMED

Class IVD General (EU MDR)

Ref MY00143CModel IA2, 50 Tests/KitRef MY00194Model IA2, 100 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Autoimmune Reagent Kit, IA2 EUDAMED
Device Name
BioCLIA Autoimmune Reagent Kit, IA2 EUDAMED
Model / Reference
IA2, 50 Tests/Kit EUDAMED
MY00143C EUDAMED
IA2, 100 Tests/Kit EUDAMED
MY00194 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030415884 EUDAMED
06924030403096 EUDAMED
Basic UDI-DI
B-06924030415884 EUDAMED
B-06924030403096 EUDAMED
EMDN Code
W0102060106 THYROSIN PHOSPHATASE IA2 ANTIBODIES 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, IA2 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000023974
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 2cd98c14-aecd-49e2-9389-6c664de02627 61 fields · synced Aug 4, 2026
  • EUDAMED 14a39b97-2cad-4da4-aed5-babd19f8fe10 61 fields · synced May 18, 2026