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Ozodrop 8 mL - ENG

by FB VISION S.p.A. Italy EUDAMED

Ref 10571720ENGModel OZODROP EMDN Q02030206

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805116070FT702OzodropMS Basic UDI-DIDate4 Mar 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  • Withdrawn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European Union — CE/MDR Withdrawn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: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Ozodrop
Model / Reference
OZODROP, 10571720ENG
Primary DI / UDI-DI
08051160700790
Basic UDI-DI
805116070FT702OzodropMS
EMDN Code
Q02030206 Eye lubricant solutions
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IT-MF-000020083

Other devices from FB VISION S.p.A.

See all devices from FB VISION S.p.A. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • CMR Substance
  • Measuring Function
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 466a94ea-9c02-4fe6-af45-19944d5b2bca 61 fields · synced 23 Oct 2026