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BioCLIA Autoimmune Reagent Kit, human tTG IgA

EUDAMED

Class IVD General (EU MDR)

Ref MY00138CModel human tTG IgA, 50 Tests/KitRef MY00189Model human tTG IgA, 100 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Autoimmune Reagent Kit, human tTG IgA EUDAMED
Device Name
BioCLIA Autoimmune Reagent Kit, human tTG IgA EUDAMED
Model / Reference
human tTG IgA, 50 Tests/Kit EUDAMED
MY00138C EUDAMED
human tTG IgA, 100 Tests/Kit EUDAMED
MY00189 EUDAMED

Identifiers

Primary DI / UDI-DI
06924030415839 EUDAMED
06924030403041 EUDAMED
Basic UDI-DI
B-06924030415839 EUDAMED
B-06924030403041 EUDAMED
EMDN Code
W0102100601 TISSUE TRANSGLUTAMINASE 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, human tTG IgA 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 2358f481-a142-44ba-9312-0390c4800429 61 fields · synced Jul 14, 2026
  • EUDAMED f69732db-0543-4d42-8d25-7b0526ea466d 61 fields · synced May 18, 2026