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Afi

EUDAMED

Class A (EU MDR)

Ref AFI-CI060V/IVD

by AFI Centrifuge

Identity

Trade Name
AFI EUDAMED
Device Name
ISA Ventilated Centrifuge, 120V 60Hz EUDAMED
Model / Reference
AFI-CI060V/IVD EUDAMED

Identifiers

Primary DI / UDI-DI
03760369880091 EUDAMED
Basic UDI-DI
376036988CI060V7Y EUDAMED
Direct Marketing DI
03760369880091 EUDAMED
EMDN Code
W02069003 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

Afi 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 41739a6a-b8a8-4833-ab54-c492a8695c14 61 fields · synced Jun 19, 2026