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ABX Minocal

EUDAMED

Class B (EU MDR)

Ref 1212032002Model 2032002

by Horiba Abx Sas

Identity

Trade Name
ABX Minocal EUDAMED
Device Name
ABX Minocal EUDAMED
Model / Reference
2032002 EUDAMED
1212032002 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230008577 EUDAMED
Basic UDI-DI
361023minocalJC EUDAMED
EMDN Code
W0103010507 WHOLE BLOOD CALIBRATORS EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

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

ABX Minocal 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 bd645b2f-6f52-4dde-8024-465b03592b37 61 fields · synced Jul 9, 2026