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Karaoğlu

by Karaoğlu Baskül Ve Cerrahi̇ Aletler İmal. San. Ti̇c. Ltd. Şti̇ EUDAMED

Active European Union

Ref KU128.02Model KARAOĞLU

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8699041KARAOGLU2040QY Basic UDI-DIDate10 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Reamers
Model / Reference
KARAOĞLU, KU128.02
Primary DI / UDI-DI
08699041107544
Basic UDI-DI
8699041KARAOGLU2040QY
EMDN Code
L1104 Bits for neurosurgery drills, reusable
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000041867

Other devices from Karaoğlu Baskül Ve Cerrahi̇ Aletler İmal. San. Ti̇c. Ltd. Şti̇

See all devices from Karaoğlu Baskül Ve Cerrahi̇ Aletler İmal. San. 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