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Afi

by AFI Centrifuge 19 variants

Ref AFI-C200V/IVD

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number376036988C200V5E Basic UDI-DI 03760369880114UDI-DIDate6 Sep 2022RegisteredStatusActive EUDAMED: not on the EU market

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
LISA Ventilated Centrifuge, 120V IVD
Model / Reference
AFI-C200V/IVD
Primary DI / UDI-DI
03760369880114
Basic UDI-DI
376036988C200V5E
Direct Marketing DI
03760369880114
EMDN Code
W02069003 Centrifuges
Device Class
Class A

Manufacturer details

EUDAMED SRN
FR-MF-000001636

Related devices

Category: General-purpose centrifuge IVD

Other devices from AFI Centrifuge

See all devices from AFI Centrifuge →

Properties

Other properties (11)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No