Skip to content

Ogm®

by Ormed Grup Medikal Turizm Sağlık Hizmetleri Sanayi ve Ticari LTD.ŞTİ EUDAMED

Active European Union

Ref KFP290326

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8682024KFP290326SY Basic UDI-DIDate22 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Ogm Bone Filler Bone Filling Cannula
Model / Reference
KFP290326
Primary DI / UDI-DI
08682024000475
Basic UDI-DI
8682024KFP290326SY
EMDN Code
P099002 Orthopaedic cement preparation and application devices and kits
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000021263

Other devices from Ormed Grup Medikal Turizm Sağlık Hizmetleri Sanayi ve Ticari LTD.ŞTİ

See all devices from Ormed Grup Medikal Turizm Sağlık Hizmetleri Sanayi ve Ticari LTD.ŞTİ →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: 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