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LISA reversible centrifuge, 120V IVD

EUDAMED

Class A (EU MDR)

Ref AFI-C200RH/IVD

by AFI Centrifuge

Identity

Device Name
LISA reversible centrifuge, 120V IVD EUDAMED
Model / Reference
AFI-C200RH/IVD EUDAMED

Identifiers

Primary DI / UDI-DI
03760369880213 EUDAMED
Basic UDI-DI
376036988C200RHZL EUDAMED
Direct Marketing DI
03760369880213 EUDAMED
EMDN Code
W02069005 REFRIGERATED CENTRIFUGES EUDAMED

Classification

Device Class
Class A 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

LISA reversible centrifuge, 120V IVD by AFI Centrifuge — 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
AFI Centrifuge
EUDAMED SRN
FR-MF-000001636

Sources (1)

  • EUDAMED 86eac108-fccc-4f1a-bf05-2e666297e1d8 61 fields · synced Jul 9, 2026