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Yumizen G1500

EUDAMED

Class A (EU MDR)

Ref 1300036330

by Horiba Abx Sas

Identity

Trade Name
Yumizen G1500 EUDAMED
Device Name
Yumizen G1500 EUDAMED
Model / Reference
1300036330 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230008300 EUDAMED
Basic UDI-DI
361023ymz_g15x0QK EUDAMED
Direct Marketing DI
03610230008300 EUDAMED
EMDN Code
W0202020102 AUTOMATED COAGULOMETERS EUDAMED

Classification

Device Class
Class A 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 G1500 by Horiba Abx Sas — Class A — 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 7e2c2a97-78b7-47cd-a560-0d4e03812859 61 fields · synced Jul 14, 2026