Skip to content

Liner X-PE Vit.E

by Lincotek Bologna S.r.l EUDAMED

Active European Union

Ref BO76.1785.000.00Model Liner X-PE Vit.E Lipped D.40 G

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08050507910977 Basic UDI-DIDate9 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  • Withdrawn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
Liner X-PE Vit.E
Model / Reference
Liner X-PE Vit.E Lipped D.40 G, BO76.1785.000.00
Primary DI / UDI-DI
08050507910977
Basic UDI-DI
B-08050507910977
Direct Marketing DI
08050507910977
EMDN Code
P090803040101 Standard polyethylene hip prostheses inserts
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000033944

Related devices

Category: Non-constrained polyethylene acetabular liner

Other devices from Lincotek Bologna S.r.l

See all devices from Lincotek Bologna S.r.l →

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