Ankura

Primary DI

08720214003391

Basic UDI-DI Code

B-08720214003391

Reference

LE-AAA2010B130

Device Types

Single use Sterile

Regulation

Eu Mdd

Classification

Eu Md Class 3

Status

On The Market

Manufacturer

LifeTech Scientific (Europe) B.V.

The stent graftsused in the Ankura AAA Stent Graft System are modular and comprises of three stent graft components, one Ankura AAA Stent Graft and two Ankura Cuff Stent Grafts. The modular system consists of one AAA Stent Graft and two Cuff Stent Grafts. Each component is introduced separately into the patient’s vascular system. The Ankura Stent Graft is a tube composed of ePTFE film supported by a metal mesh called a stent. The markers are fixed on the stent.The graft which is ultrathin artificial vascular material fixed to the stent without suture, can isolate aneurysm from blood, and it is stronger than the weakened artery and it allows the blood to pass through it without pushing on the bulge. The stent can provide stable and expansionary force necessary to open the graft.

Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDD).