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Alecta Posterior Polyaxial Cannulated Stabilization Screw 5, 5X40

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

Active European Union

Ref AT1204.0005540

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681087294180 Basic UDI-DIDate16 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Alecta Posterior Polyaxial Cannulated Stabilization Screw
Model / Reference
AT1204.0005540
Primary DI / UDI-DI
08681087294180
Basic UDI-DI
B-08681087294180
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.

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Properties

Show 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