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Piiloset BioDrop MD

by Oy Finnsusp Ab Finland EUDAMED

Ref F0002

EMDN Q02030206

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FIMF000011137F0002W4 Basic UDI-DIDate30 Nov 2021RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
BioDrop MD
Model / Reference
F0002
Primary DI / UDI-DI
D-FIMF000011137F0002W4
Basic UDI-DI
B-FIMF000011137F0002W4
EMDN Code
Q02030206 Eye lubricant solutions
Device Class
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 (1)

  • EUDAMED 889000cd-4508-4deb-80d9-917fccdbe535 61 fields · synced 23 Oct 2026