Other Tissue Valves
S.A.V. Aortic
Edwards Prima Plus
Aortic Porcine
S.A.V. Mitral
Duraflex Mitral
Mitral Porcine
Valved Conduit
Bovine Pericardial Patch
Related Products
Pericardial Valves
Annuloplasty Rings
Transcatheter Valves
Patient Website
Heart Valve News
Report from NPR
Request Information
Technical Information
Cardiovascular Surgery FAQ
Temperature Guidelines
MRI Safety
Heart Valve Education
Carpentier-Edwards Bioprosthetic Valved Conduit
With 25 years of proven performance
1
, the Carpentier-Edwards valved conduit is ideal for complex reconstruction with challenging congenital malformations.
Woven polyester conduit
6 cm and 9 cm extensions provide ample material for adapting to varied anatomy
Exceptional durability
Built on the exceptional durability and hemodynamics of the Carpentier-Edwards porcine aortic bioprosthesis
2,3
Eight convenient sizes
From 12-30 mm provides an ideal homograft alternative
Adaptable and modifiable
Two seam lines mark valve position and allow close cutting for precise fit
Sinus of valsalva
The use of a larger diameter valve than graft diameter along with integral sinus provides more physiological flow and valve closure characteristics
XenoLogiX treatment*
Confronts calcification using a two-step process to effectively extract the phospholipids from bioprosthetic tissue
Flexible stent
Reduces the loading shock on the leaflets and mimics the physiology and mechanics of natural heart valves
* No clinical data are available which evaluate the long-term impact of the Edwards Lifesciences tissue treatment in patients
References:
1. Butany et al. A Carpentier-Edwards porcine valved dacron conduit: At 25 years. International Journal of Cardiology 2007; 117:e1-e16.
2. Jamieson et al. Carpentier-Edwards standard porcine bioprosthesis: A 21-year experience. Ann Thorac Surg 1998;66:S40-S43
3. Bojar et al. Clinical and hemodynamic performance of the 19-mm Carpentier Edwards porcine bioprosthesis. Ann Thorac Surg 1993;56:1141-1147
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.
Model
Specifications
Contact Us
|
Legal Terms
|
Privacy Policy
| © 2012 Edwards Lifesciences LLC. All rights reserved.