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In Situ Rod Bender Left

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

Active European Union

Ref AT12002.INS033L

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681087500878 Basic UDI-DIDate16 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

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 In Situ Rod Bender Left
Model / Reference
AT12002.INS033L
Primary DI / UDI-DI
08681087500878
Basic UDI-DI
B-08681087500878
EMDN Code
L99 Surgical instruments, reusable - other
Device Class
Class I
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

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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