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Puratu

by Atilgan Tibbi̇ Ürünler Sağlik Hi̇zmetleri̇ Anoni̇m Şi̇rketi̇ 114 variants

Ref TNF.LTI.11400

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682054130562 Basic UDI-DI 08682054130562UDI-DIDate24 Apr 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  • Withdrawn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
Femoral Nail
Model / Reference
TNF.LTI.11400
Primary DI / UDI-DI
08682054130562
Basic UDI-DI
B-08682054130562
EMDN Code
P09120201 Intramedullary nails
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020009

Related devices

Category: Arthrodesis intramedullary nail, non-distracting

Other devices from Atilgan Tibbi̇ Ürünler Sağlik Hi̇zmetleri̇ Anoni̇m Şi̇rketi̇

See all devices from Atilgan Tibbi̇ Ürünler Sağlik Hi̇zmetleri̇ Anoni̇m Şi̇rketi̇ →

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