Profile: Circulatory Technology, Inc. develops medical devices to improve the safety and efficacy of cardiopulmonary bypass. Our products include The Better-Bladder™ (BB), The V-Bag™, The Better-Header™ and The Better-Venter™. The Better-Bladder™ (BB) is an inline reservoir that allows noninvasive pressure measurements, for example, during vacuum augmented venous drainage (VAVD). The BB has a standard perfusion tubing with a thin walled, sausage shaped balloon sealed within a rigid housing. The major advantage of the BB is that the measured pressure can be used as the input signal to a pump controller to stop or decrease pump speed at a chosen pressure. The second advantage of the BB is that it can be placed near the patient instead of on the floor, if the pressure set to stop/slow the pump is negative (e.g., -50 mmHg). The V-Bag™ is a disposable soft shell venous reservoir that provides a compliant volume chamber and acts as a bubble trap during procedures requiring cardiopulmonary bypass support for periods of up to six hours. It can provide VAVD or can be used for gravity drainage. The Better-Header is a disposable for the roller pump that automatically protects against over-pressurization. The Better-Venter™ is designed for use in an extracorporeal circuit to prevent excessive negative pressure during venting. It also incorporates a one-way valve in the inlet tubing to reduce the possibility of flow returning to the heart.
FDA Registration Number: 2436790
7 Products/Services (Click for related suppliers)
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• Cardiopulmonary Bypass Blood Reservoir (FDA Code: DTN / 870.4400) A cardiopulmonary bypass blood reservoir is a device used in conjunction with short-term extracorporeal circulation devices to hold a reserve supply of blood in the bypass circulation. |
• Cardiopulmonary Bypass Pressure Relief Valve (FDA Code: MNJ / 870.4400) |
• Cardiopulmonary Bypass Vascular Catheter (FDA Code: DWF / 870.4210) A cardiopulmonary bypass vascular catheter, cannula, or tubing is a device used in cardiopulmonary surgery to cannulate the vessels, perfuse the coronary arteries, and to interconnect the catheters and cannulas with an oxygenator. The device includes accessory bypass equipment. |
• Dialysis Transducer Protector (FDA Code: FIB / 876.5820) A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer. |
• Perfusion Tubings |
• Pressure Infusor for I.V. Bags (FDA Code: KZD / 880.5420) A pressure infusor for an I.V. bag is a device consisting of an inflatable cuff which is placed around an I.V. bag. When the device is inflated, it increases the pressure on the I.V. bag to assist the infusion of the fluid. |
• Venous Bags |