← Back to catalogue

BioCLIA Autoimmune Reagent Kit, AMA-M2

EUDAMED

Class IVD General (EU MDR)

Ref MY00118CModel AMA-M2, 50 Tests/Kit

by HOB Biotech Group Corp., Ltd.

Identity

Trade Name
BioCLIA Autoimmune Reagent Kit, AMA-M2 EUDAMED
Device Name
BioCLIA Autoimmune Reagent Kit, AMA-M2 EUDAMED
Model / Reference
AMA-M2, 50 Tests/Kit EUDAMED
MY00118C EUDAMED

Identifiers

Primary DI / UDI-DI
06924030415679 EUDAMED
Basic UDI-DI
B-06924030415679 EUDAMED
EMDN Code
W0102100702 ANTI-MITOCHONDRIAL ANTIBODIES 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, AMA-M2 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 (1)

  • EUDAMED 54fb7dbf-13f3-446c-97af-0691d734e7e6 61 fields · synced Jun 17, 2026