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Orti̇mplant

by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi EUDAMED

Active European Union

Ref OSI100142Model ORTİMPLANT

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8680941OHAM000014Q Basic UDI-DIDate24 Apr 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  • Withdrawn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
Buck Hammer W/Needle and Brush 180mm
Model / Reference
ORTİMPLANT, OSI100142
Primary DI / UDI-DI
08680941165994
Basic UDI-DI
8680941OHAM000014Q
Direct Marketing DI
08680941165994
EMDN Code
L160199 Diagnostic hammers, reusable - other
Device Class
Class I
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
TR-MF-000017438

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Properties

  • Reusable
  • Administering Medicine
  • Measuring Function

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Incorporates Medicinal Product: No