

IntraClude device
The IntraClude intra-aortic occlusion device is indicated for use in patients undergoing cardiopulmonary bypass. The IntraClude intra-aortic occlusion device occludes and vents the ascending aorta when the balloon is inflated. The device’s central lumen allows delivery of cardioplegia to arrest the heart. The pressure lumen allows monitoring of the aortic root pressure.
- 10.5 Fr (3.5 mm), triple-lumen, 100 cm long catheter
- Designed to occlude the ascending aorta in order to partition the aortic root from arterial circulation
- Balloon expands to occlude a range of aorta sizes from 20 to 40 mm
- Designed to be used in the femoral approach with:
- 21 Fr Edwards EndoReturn arterial cannula (ER21B)
- 23 Fr Edwards EndoReturn arterial cannula (ER23B)
- 19 Fr Edwards introducer sheath (IS19A)
- The shaft is provided with an extended strain relief designed to prevent kinking
Contents:
- 1 IntraClude intra-aortic occlusion device
- 1 Syringe (35 ml)
- 1 Guidewire (200 cm)
- 1 Blue stripe pressure tubing
- 1 Red stripe pressure tubing
IntraClude device
IntraClude DEVICE
IntraClude device features
IntraClude Device Features
Arterial perfusion flow vs pressure
Arterial Perfusion Flow vs Pressure
IntraClude device
IntraClude DEVICE




IntraClude device features
IntraClude Device Features

Arterial perfusion flow vs pressure
Arterial Perfusion Flow vs Pressure

Model | Description | Size | Image |
---|---|---|---|
ICF100 | IntraClude intra-aortic occlusion device | 10.5 Fr | ![]() |
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Important safety information
See Instructions For Use (IFU) / Directions For Use (DFU) for full prescribing information, including indications, contraindications, warnings, precautions and adverse events.
Important safety information
Caution: Federal (United States) law restricts this device to sale by or on the order of a physician.
See Instructions For Use (IFU) / Directions For Use (DFU) for full prescribing information, including indications, contraindications, warnings, precautions and adverse events.
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