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Innodrops F1a (GOF1aM-001)

by Enable Innovations SRL EUDAMED

Withdrawn Not intended for the EU market

Ref 050208, 050155, 050207Model Gocce oculari Innodrops F1a

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80540851201NH Basic UDI-DIDate20 Apr 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030020-01 Supplemented

    Quality management system EU MDR

    Notified body
    ICIM S.P.A. 0425
    Issued
    26 Mar 2025
    Expires
    26 Feb 2028
    Reason
    Other

Specification

EUDAMED

Device Name
Gocce oculari Innodrops F1a
Model / Reference
Gocce oculari Innodrops F1a, 050208, 050155, 050207
Primary DI / UDI-DI
08054085120230, 08054085120100, 08054085120223

Manufacturer details

EUDAMED SRN
IT-MF-000026066

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