← Back to catalogue

Yumizen G Cuvettes

EUDAMED

Class A (EU MDR)

Ref 1300036425

by Horiba Abx Sas

Identity

Trade Name
Yumizen G Cuvettes EUDAMED
Device Name
Yumizen G Cuvettes EUDAMED
Model / Reference
1300036425 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230008492 EUDAMED
Basic UDI-DI
361023ymz_g_cuvettesCX EUDAMED
EMDN Code
W0503010203 SAMPLES ANALYSES, PLASTIC CUVETTES 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

No

EUDAMED

New Device

No

EUDAMED

Yumizen G Cuvettes 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (1)

  • EUDAMED d2d3ca52-e9d5-411b-9c41-f4b1b4ddbfa0 61 fields · synced Jun 19, 2026