eSheath Expandable Introducer Sheath
Transcatheter Heart Valves
Aortic
Edwards SAPIEN XT
NovaFlex+
Ascendra2

Pulmonic
Edwards SAPIEN Pulmonic

Clinical
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eSheath Expandable Introducer Sheath
eSheath
Expandable Introducer Sheath
The only introducer sheath that combines a low (16F) profile
with dynamic expansion


eSheath Expandable Introducer Sheath
The Edwards dynamic expansion mechanism

The sheath’s low profile and Dynamic Expansion Mechanism (DEM)set the
Edwards eSheath apart. This unique combination of features is designed to
minimize access vessel trauma and to facilitate smooth valve delivery with
no extra procedural steps required.




Designed to reduce vascular trauma

The Edwards eSheath features the innovative Dynamic Expansion Mechanism (DEM) that allows for transient sheath expansion
during valve delivery. Immediately after the Edwards SAPIEN XT Transcatheter Heart valve passes through the sheath, the DEM
allows the sheath to return to a low profile diameter. This reduces the time the access vessel is expanded, thereby minimizing
the risk of vascular trauma.
Designed to reduce vascular trauma
The lower profile of the 16F Edwards eSheath is designed to reduce trauma on access vessel entry and exit. The lower profile of the 16F Edwards eSheath is designed to reduce trauma on access vessel entry and exit.
Edwards NovaFlex Introducer Sheath Edwards eSheath
The lower profile of the 16F Edwards eSheath is designed to reduce trauma on access vessel entry and exit.


Allows for retrievability

If necessary, the DEM feature allows for the retrieval of the Edwards SAPIEN XT Transcatheter Heart valve prior to valve deployment.1


Reduced push force

The DEM feature combined with the eSheath’s coated inner lining, that has a low-coefficient of friction, reduces the push force through the shaft during device insertion by up to 40%.2



References
1. After valve alignment procedure, based on bench and animal testing.
2. When compared to the NovaFlex Introducer Sheath tested with 9350FS23.
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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