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Ogm®

by Ormed Grup Medikal Turizm Sağlık Hizmetleri Sanayi ve Ticari LTD.ŞTİ 8 variants

Ref 1406/VTB

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682024000130 Basic UDI-DI 08682024000130UDI-DIDate21 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
OGM Vertebroplasty Bone Cement 25 g
Model / Reference
1406/VTB
Primary DI / UDI-DI
08682024000130
Basic UDI-DI
B-08682024000130
EMDN Code
P900403 Non-resorbable filling and reconstruction devices
Device Class
Class III
EU 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
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No