← Back to catalogue

BioCLIA Autoimmune Reagent Kit, Ro52

EUDAMED

Class IVD General (EU MDR)

Ref MY00104CModel Ro52, 50 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, 50 Tests/Kit EUDAMED
MY00104C EUDAMED

Identifiers

Primary DI / UDI-DI
06924030415532 EUDAMED
Basic UDI-DI
B-06924030415532 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

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, 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

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 5c2b65aa-575c-41c2-ba23-4faea5b56b00 61 fields · synced Jun 18, 2026