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 features

Arterial perfusion flow vs pressure

INTRA-AORTIC OCCLUSION DEVICE
Arterial Perfusion Flow vs. Pressure
INTRA-AORTIC OCCLUSION DEVICE

IntraClude device features

Arterial perfusion flow vs pressure

Arterial Perfusion Flow vs. Pressure

IntraClude device brochure

Youtube Video

IntraClude intra-aortic occlusion device prep video

Short video demonstrating preparation of the IntraClude intra-aortic occlusion device

ModelDescriptionSizeImage
ICF100 IntraClude intra-aortic occlusion device 10.5 Fr

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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.

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.

Important safety information

Important safety information

Important Safety Information: Carpentier-Edwards PERIMOUNT Aortic Bioprostheses

Indications: For use in patients whose aortic valvular disease warrants replacement of their natural or previously placed prosthetic valve.

Contraindications: Do not use if surgeon believes it would be contrary to the patient’s best interests.

Complications and side effects: Stenosis, regurgitation, endocarditis, hemolysis, thromboembolism, valve thrombosis, nonstructural dysfunction, structural valve deterioration, anemia, arrhythmia, hemorrhage, transient ischemic attack/stroke, congestive heart failure, myocardial infarction, angina, any of which could lead to reoperation, explantation, permanent disability, and death.

CAUTION: Federal (USA) law restricts these devices to sale by or on the order of a physician. See instructions for use for full prescribing information.

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