

Minimal incision
MVR / AVR
- Less traumatic aortic occlusion than cross-clamping
- Antegrade cardioplegia delivery
- Aortic root venting for an unobstructed, virtually bloodless surgical field
- Aortic root pressure monitoring
*When compared to median sternotomy
IntraClude device
IntraClude device features
Arterial perfusion flow vs pressure
IntraClude device




IntraClude device features

Arterial perfusion flow vs pressure

IntraClude intra-aortic occlusion device prep video
Short video demonstrating preparation of the IntraClude intra-aortic occlusion device
Model | Description | Size | Image |
---|---|---|---|
ICF100 | IntraClude Intra-aortic Occlusion Device | 10.5 Fr | ![]() |
- Delivery of retrograde cardioplegia solution, outside of the incision
- Occlusion of the coronary sinus
- Monitoring of coronary sinus pressure
- Highly engineered, 9 Fr. shaft designed for excellent control and device management
- Specially designed, 59 cm, steerable shaft with depth markers and orientation line for ease of placement
ProPlege device
Articulating-positions
Diameter vs volume
ProPlege device




Articulating-positions

Diameter vs volume

Model | Description | Size | Image |
---|---|---|---|
PR9 | ProPlege Peripheral Retrograde Cardioplegia Device | 9 Fr | ![]() |
- Percutaneous insertion via internal jugular vein provides an unobstructed operative field
- Thin wall, 8.3 Fr design delivers high flow rates to ensure adequate venting in all sizes of patients
- Contamination guard system facilitates sterile catheter repositioning
- Pre-shaped catheter and flow directed balloon enable easy placement into the pulmonary artery
EndoVent device
EndoVent device


Model | Description | Size | Image |
---|---|---|---|
EV | EndoVent Pulmonary Catheter | 8.3 Fr | ![]() |
The Edwards Advantage
We are committed to providing your institution, clinicians and staff with the highest levels of customer service and support.
You are busy – We are flexible
Indicate your topics of interest and preferred communication frequency
For professional use
See instructions for use for full prescribing information, including indications, contraindications, warnings, precautions and adverse event.
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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