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19 December 2024
In coronary bypass surgery, precision and control are paramount. Enclose® II Proximal Anastomosis Assist Device from Peters Surgical is designed to enhance these aspects, ensuring a seamless and hemostatic process during graft placement. This article provides an overview of the Enclose® II device, its composition, and its step-by-step application in coronary bypass surgery.
Enclose® II device is engineered to facilitate proximal anastomosis:
Enclose® II device is used to streamline the process of proximal anastomosis, ensuring a precise and hemostatic seal. Here is a step-by-step guide to its application:
The use of Enclose® II device allows the surgeon to perform anastomosis using hand suturing techniques without the use of side biting clamps, thus reducing the potential of neurological deficits. Traditional steel jaw partial occlusion clamps increase the potential for acute traumatic injury to the vessel and embolization, thus increasing procedure risk.
Enclose® II proximal anastomosis assist device highlight Peters Surgical’s commitment provide high quality medical device for patient care. Its precision, reliability, and ease of use make it an essential device for coronary bypass surgery, ensuring optimal outcomes and improved patient care.
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Legal mentions
Enclose® II Anastomosis Assist Device
INDICATIONS:
The Enclose® II device is intended for use by cardiac surgeons during on-pump or off-pump coronary artery bypass grafting (CABG) procedures in place of partial occlusion clamps in ascending aortas free of atheromatous disease. Medical Device Class IIa – CE 2797 – Manufacturer: Vitalitec International Inc. Carefully read the instructions for use of the medical device before use.