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Femoral Head Adapter

by Lincotek Bologna S.r.l EUDAMED

Active European Union

Ref BO76.3124.000.00Model Femoral Head Ceramic Biolox®Delta Revision 16/18 Adapter L +4

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08050391091943 Basic UDI-DIDate5 Dec 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Femoral Head Adapter
Model / Reference
Femoral Head Ceramic Biolox®Delta Revision 16/18 Adapter L +4, BO76.3124.000.00
Primary DI / UDI-DI
08050391091943
Basic UDI-DI
B-08050391091943
Direct Marketing DI
08050391091943
EMDN Code
P090804050299 Femoral heads for primary implant of total prostheses - other
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000033944

Other devices from Lincotek Bologna S.r.l

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Properties

Show properties
  • Sterile
  • Implantable
Other properties (11)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: 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