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Piiloset BioTwin

by Oy Finnsusp Ab Finland EUDAMED

Ref F0006

EMDN Q02030204

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FIMF000011137F0006WC Basic UDI-DIDate2 Dec 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 22 Oct 2026

Device Name
BioTwin
Model / Reference
F0006
Primary DI / UDI-DI
D-FIMF000011137F0006WC
Basic UDI-DI
B-FIMF000011137F0006WC
EMDN Code
Q02030204 Contact lenses storing and cleaning 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 2bc9f675-bcc8-4df8-8ac2-cda135ca5914 61 fields · synced 22 Oct 2026