Skip to content

Alecta Posterior Polyaxial Cannulated Spondylolisthesis Stabilization Screw 8, 0X45

by Li̇gamed Tibbi̇ Malzemeler San. Ve Ti̇c. Ltd. Şti̇. EUDAMED

Active European Union

Ref AT1206.0008045

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681087296979 Basic UDI-DIDate16 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Alecta Posterior Polyaxial Cannulated Spondylolisthesis Stabilization Screw
Model / Reference
AT1206.0008045
Primary DI / UDI-DI
08681087296979
Basic UDI-DI
B-08681087296979
EMDN Code
P09070302 Thoracolumbosacral fixation systems
Device Class
Class IIb
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000015834

Other devices from Li̇gamed Tibbi̇ Malzemeler San. Ve Ti̇c. Ltd. Şti̇.

See all devices from Li̇gamed Tibbi̇ Malzemeler San. Ve Ti̇c. Ltd. Şti̇. →

Properties

  • Implantable

Other properties (12)

  • Sterile: No
  • 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