Ankura
Basic Information
- Primary DI
- 08720214004503
- Basic UDI-DI Code
- B-08720214004503
- Reference
- LE-cuff1416C090
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- LifeTech Scientific (Europe) B.V.
Additional Description
The Ankura Cuff Stent Graft is pre-loaded into the Delivery System. The loaded delivery system is inserted endoluminally via the femoral or iliac artery and tracked through the patientโs vasculature to deliver the stent graft to the target site. The Ankura stent graft is a tube composed of ePTFE film supported by a metal mesh called a 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 stabile and expansionary force necessary to open the graft.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P070401020101 | PTFE VASCULAR ENDOPROSTHESES, STRAIGHT - ABDOMINAL |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II Section 4 | 2166785CE03&2166785DE11 | DEKRA Certification B.V. |
Available In Countries
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDD).