Ascendra2 Transapical System
Transcatheter Heart Valves
Aortic
Edwards SAPIEN XT
NovaFlex+
Ascendra2
Overview
Procedural Animation

Pulmonic
Edwards SAPIEN Pulmonic

Clinical
The PARTNER Trial Results

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Ascendra2 Transapical System

Control

Optimized working length designed for transapical access

Precision

Balloon-expandable design allows for user-controlled
inflation and precise delivery

Stability

Reinforced sheath design provides added control
during delivery
24F Introducer Sheath
The lowest profile transapical device*
  • Enhances access and improves closure
Integrated seal technology
  • Provides hemostatic control during insertion and tracking
Minimized risk of left ventricular trauma
  • Establishes an access route through the left ventricle to the aortic valve
  • Soft distal tip reduces risk of trauma during insertion


The Complete Edwards Transapical System

Edwards SAPIEN XT Transcatheter Heart Valve

Designed for predictable performance

Ascendra2 Delivery System

Engineered for enhanced procedural control
Product Name 23 mm 26 mm
Ascendra2 Transapical Kit 9350AS223 9350AS226
Edwards SAPIEN XT Transcatheter Heart Valve 9300TFX
(23 mm)
9300TFX
(26 mm)
Ascendra2 Delivery System 9350AS23 9350AS26
Ascendra2 Introducer Sheath Set 9320IS24 9320IS24
Ascendra Balloon Aortic Valvuloplasty Catheter 9100BAVC 9100BAVC
Crimper 9350CR 9350CR
Atrion QL2530 Inflation Device 96402 96402
Product Name 29 mm
Ascendra Transapical Kit 9350AS129
Edwards SAPIEN XT Transcatheter Heart Valve 9300TFX
(29 mm)
Ascendra Balloon Catheter 9350BCL29
Ascendra Introducer Sheath Set 9100IS
Ascendra Balloon Aortic Valvuloplasty Catheter 9100BAVC
Crimper 9350CR
Atrion Inflation Device 96313
96402
*Among products commercially available as of January 2012.
† First-generation Ascendra. Not commercialized.
For professional use. See instructions for use for full prescribing information, including indications, contraindications, warnings, precautions and adverse events.

Edwards Lifesciences devices placed on the European market meeting the essential requirements referred to in Article 3 of the Medical Device Directive 93/42/EEC bear the CE marking of conformity.
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