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Yumizen Compressor

EUDAMED

Class A (EU MDR)

Ref 1300080584

by Horiba Abx Sas

Identity

Trade Name
Yumizen Compressor EUDAMED
Device Name
Yumizen Compressor EUDAMED
Model / Reference
1300080584 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230013472 EUDAMED
Basic UDI-DI
361023ymz_compressorN9 EUDAMED
Direct Marketing DI
03610230013472 EUDAMED
EMDN Code
W0580 IVD GENERAL USE CONSUMABLES DEVICES - OTHER ACCESSORIES 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 Compressor 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 c890ad05-4a7e-4a37-b9b6-b7a5cf57e15c 61 fields · synced Jul 8, 2026