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Yumizen H500 CT

EUDAMED

Class B (EU MDR)

Ref 1300092722, 1300092723, 1300092724, 1300092725

by Horiba Abx Sas

Identity

Trade Name
Yumizen H500 CT EUDAMED
Device Name
Yumizen H500 CT EUDAMED
Model / Reference
1300092722, 1300092723, 1300092724, 1300092725 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230009352 EUDAMED
Basic UDI-DI
361023ymz_h500_ctLS 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 CT 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 (2)

  • EUDAMED 7da943c6-2fe1-4df4-ba07-578fa51548b7 61 fields · synced Oct 6, 2026
  • EUDAMED 7da943c6-2fe1-4df4-ba07-578fa51548b7-1 61 fields · synced Jun 10, 2026