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Kibo

by Li̇nacol Medi̇kal A.Ş. Türkiye EUDAMED

Ref KICP-001

EMDN Z12039001

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08683955400129 Basic UDI-DIDate28 Mar 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
KIBO Ventriküler Kafa İçi Basınç Ölçüm Cihazı / KIBO Ventricular Intracranial Pressure Measurement Device
Model / Reference
KICP-001
Primary DI / UDI-DI
08683955400129
Basic UDI-DI
B-08683955400129
EMDN Code
Z12039001 Intracranial pressure measuring systems
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000033766

Other devices from Li̇nacol Medi̇kal A.Ş.

See all devices from Li̇nacol Medi̇kal A.Ş. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
  • Measuring Function
Other properties (8)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 792e96a4-a08f-42e2-baff-8b0df3ef8c83 61 fields · synced 22 Oct 2026