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Marker ArUco Femur

by Orthokey Italia SRL FDA registration: Italy EUDAMED

Ref 20905000FModel ORTHOKEY Surgical instruments I EMDN L0999

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805267596SurgicalInstC1LV Basic UDI-DIDate23 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
ORTHOKEY Surgical instruments I, 20905000F
Primary DI / UDI-DI
08052675960259
Basic UDI-DI
805267596SurgicalInstC1LV
Direct Marketing DI
08052675960259
EMDN Code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000026488

Other devices from Orthokey Italia SRL

See all devices from Orthokey Italia SRL →

Properties & raw data

Show properties, registry sources and raw records
  • Reprocessed
Other properties (12)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 1c936077-7c5a-4091-b3fa-19a850fa9384 61 fields · synced 22 Oct 2026