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Orti̇mplant

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

Ref O1200-0117Model ORTİMPLANT

EMDN L0903

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8683206OHAM00001Z2 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 22 Oct 2026

Device Name
Mallet Remov-Discs 135g 25mm 18.5 Cm
Model / Reference
ORTİMPLANT, O1200-0117
Primary DI / UDI-DI
08683206673562
Basic UDI-DI
8683206OHAM00001Z2
EMDN Code
L0903 Orthopaedic surgery hammers, 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

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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 e7abaf49-0e07-480b-b612-b56c95a44736 61 fields · synced 22 Oct 2026