Abstract: A locking component for locking a medical device onto a guide wire. Such medical devices include, for example, an embolic filter assembly used to capture embolic material that may be created and released into a patient's vasculature during a stenting or angioplasty procedure. The embolic filter assembly tracks along the guide wire, and is delivered to a treatment site where it is locked in place and deployed. The locking component enables the filter assembly to lock onto any standard guide wire, and does not require a modified guide wire that has a specially-designed fitting or stop to accomplish the locking function.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: A method and apparatus for applying a polymer coating on an elongated substrate, preferably an elongate intracorporeal device in the form of a guidewire. An extrudable polymer cartridge is moved by a cartridge advancement mechanism into a guide chamber which is heated at an end with a die or orifice through which a desired portion of a guidewire may pass and be coated. Parameters such as guide chamber temperature, pull speed and force exerted by the cartridge advancement mechanism may be controlled with a computer program in order to achieve repeatable results. The guide chamber, extrudable polymer cartridge, die, and push tube may all be made from polymer components which can be reused or disposed of after a single use.

Abstract: An apparatus for determining whether an IV infusion set has infiltrated the tissue of a patient includes a pump for pumping fluid through the IV set into the patient and a pressure transducer operably engaged with the IV set between the pump and patient. The pressure transducer is electrically connected to a microprocessor, and the microprocessor is electrically connected to the motor of the pump to control the pump to alternately withdraw from and infuse into the patient a predetermined volume of fluid.This predetermined volume of fluid is withdrawn from the patient by the pump at a preselected withdrawal pressure, while the pump infuses the predetermined volume of fluid into the patient at a preselected infusion pressure. The microprocessor measures both the time period for infusing the predetermined volume of fluid and the time period for withdrawing the predetermined volume of fluid. Based upon these time periods, the microprocessor evaluates whether the IV set has infiltrated the patient's tissue.

Abstract: A linear peristaltic pump includes a mechanism for maintaining linear flow of fluid through an I.V. tube. The mechanism comprises a casing carrying a rotatable camshaft having a plurality of cams spaced therealong in helical arrangement and a plurality of fingers coupled to the camshaft. A housing for establishing linear reciprocal movement of the fingers in response to rotation of the shaft establishes a moving zone of occlusion along a tube held against the fingers. Aligning means are included for establishing an axis of rotation of the camshaft which is slightly tilted with respect to the tube. This is accomplished by raising or lowering the upstream or the downstream end of the camshaft to prevent unwanted pressure from building up in the tube to reduce pulsatile flow and maintain linear flow. The aligning mechanism comprises a generally cylindrical bushing having an eccentric hole therethrough for carrying the hinged connection between the casing and the housing.

Abstract: A linear peristaltic pump equipped with a pressure relief mechanism for pumping I.V. fluids to a patient comprises a platen for supporting the tube, and a plurality of fingers which sequentially urge against the tube resting against the platen for creating a moving zone of occlusion. Cam lobes are formed to lift a penultimate and ultimate finger off of the tube at a rate faster than the other fingers to prevent pressure increases inside the tube which would otherwise be caused by other fingers urging against the tube. Additionally, the ultimate finger may be shortened with respect to the other fingers to reduce the total occlusion time of the ultimate finger to provide a more linearized flow of fluid to the patient.

Abstract: A peristaltic pump for infusing medical solutions to a patient through a flexible tube comprises a pair of counter-rotating drive shafts mounted on a base. A separate roller is eccentrically mounted on each of the drive shafts and each roller has a wheel which is slidingly suspended at its periphery. A pair of curvilinear platens are each separately disposed concentric with a respective drive shaft to engage the tube between the wheel on each roller and the platen. Cooperative counterrotation of the drive shafts cause each roller to sequentially squeeze the tube against its respective platen to create a moving zone of occlusion along the tube.

Abstract: A device for detecting partial restriction in a fluid line connecting a fluid source with an IV infusion pump comprises a gauge mounted on the pump and operatively associated with the line to determine fluid pressure therein. The pump also comprises a peristable finger to conditionally occlude the line and a miroprocessor, upon occlusion of the line, to establish fluid pressure parameters within which the indication is that there is no partial restriction in the line. The pump also uses the microprocessor to compare actual pressure measured by the gauge during an occlusion with the established parameters to determine whether pump operation is to be continued.