Skip to content

Duplex

by Adler Ortho S.p.A Italy EUDAMED

Ref 0772262Model FIXA DUPLEX DUAL MOBILITY CEMENTED CUP SIZE 62

EMDN P090803050101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08052532837809 Basic UDI-DIDate4 Jun 2026RegisteredStatusActive

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

Model / Reference
FIXA DUPLEX DUAL MOBILITY CEMENTED CUP SIZE 62, 0772262
Primary DI / UDI-DI
08052532837809
Basic UDI-DI
B-08052532837809
EMDN Code
P090803050101 Cemented double-mobility acetabular cups
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000010164

Other devices from Adler Ortho S.p.A

See all devices from Adler Ortho S.p.A →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • 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 9a118447-0431-4357-be52-22ed3c24ca5a 61 fields · synced 23 Oct 2026