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Fitostill plus

by Aboca S.P.A. Società Agricola 7 variants

Ref 08032472009498

Active European Union

CE MDR

Valid until

2 Nov 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Eurofins Product Testing Italy S.r.l.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8032472FISTIax1AS Basic UDI-DI 08032472009498UDI-DIDate27 Mar 2024RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.23/5275 Active

    Quality management system EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    3 Nov 2023
    Expires
    2 Nov 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
08032472009498
Primary DI / UDI-DI
08032472009498
Basic UDI-DI
8032472FISTIax1AS
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIb
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000029499

Other devices from Aboca S.P.A. Società Agricola

See all devices from Aboca S.P.A. Società Agricola →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No