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Yumizen H500 CRP

EUDAMED

Class B (EU MDR)

Ref 1300148023Model Yumizen H500 CRP

by Horiba Abx Sas

Identity

Trade Name
Yumizen H500 CRP EUDAMED
Device Name
Yumizen H500 CRP EUDAMED
Model / Reference
Yumizen H500 CRP EUDAMED
1300148023 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230009741 EUDAMED
Basic UDI-DI
361023ymz_h500CRPDY EUDAMED
EMDN Code
W0202010101 AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - LOW ROUTINE (Throughput <= 100 samples/hr) EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Yumizen H500 CRP by Horiba Abx Sas — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (1)

  • EUDAMED 677baa92-a7ed-460d-8854-d35c359a3ded 61 fields · synced Jun 18, 2026