Skip to content

Orti̇mplant

by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi Türkiye EUDAMED

Ref OSI100372Model ORTİMPLANT

EMDN L0102

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8680941OCUT00001F8 Basic UDI-DIDate24 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Ulrich Fistula Knife Hollow 225mm
Model / Reference
ORTİMPLANT, OSI100372
Primary DI / UDI-DI
08680941167820
Basic UDI-DI
8680941OCUT00001F8
Direct Marketing DI
08680941167820
EMDN Code
L0102 Surgical knives, reusable
Device Class
Class I
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
TR-MF-000017438

Other devices from Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi

See all devices from Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 1d8b5fbe-7a14-40bf-8b60-35897dafd66c 61 fields · synced 24 Oct 2026