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Disior Bonelogic 1.0

by Disior Oy EUDAMED

Withdrawn No longer placed on the EU market

Ref Bonelogic Ortho Foot and AnkleModel Bonelogic 1.0

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06429810209016 Basic UDI-DIDate21 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  • Withdrawn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European Union — CE/MDD Withdrawn

No EU certificate is linked to this device in EUDAMED.

Specification

EUDAMED

Device Name
Bonelogic Ortho Foot and Ankle
Model / Reference
Bonelogic 1.0, Bonelogic Ortho Foot and Ankle
Primary DI / UDI-DI
06429810209016
Basic UDI-DI
B-06429810209016
EMDN Code
Z110603 Picture archiving and communication systems
Device Class
Class IIb
Special Device Type
-1192
Market of Registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000002448

Other devices from Disior Oy

Properties

  • Measuring Function

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No