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Piiloset BioDrop

by Oy Finnsusp Ab Finland EUDAMED

Ref F0001, F0016 EMDN Q02030206

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FIMF000011137F0001W2 Basic UDI-DIDate2 Dec 2021RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
BioDrop SD
BioDrop Plus SD
Model / Reference
F0001, F0016
Primary DI / UDI-DI
D-FIMF000011137F0001W2, D-FIMF000011137F0016WF
Basic UDI-DI
B-FIMF000011137F0001W2, B-FIMF000011137F0016WF
EMDN Code
Q02030206 Eye lubricant solutions
Device Class
Class IIa
Class IIb
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000011137

Other devices from Oy Finnsusp Ab

See all devices from Oy Finnsusp Ab →

Properties & raw data

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

Sources (2)

  • EUDAMED 7a939eb2-726a-4e89-a5e4-8b5acd54f2f8 61 fields · synced 24 Oct 2026
  • EUDAMED D-FIMF000011137F0016WF|B-FIMF000011137F0016WF 61 fields · synced 18 May 2026