An artificial heart for use in a human recipient includes a housing within which a quartet of turbine pump segments are operative. The quartet of turbine pump segments is configured to provide a pair of redundant input and output turbine pump segment pairs each input and output pair being coupled by a curved passage providing a redundancy which, in turn, enhances the safety factor provided by the artificial heart. A controller is powered by a rechargeable battery and is operative to apply appropriate drive signals to the motor drives of the turbine pump segments. The battery may be implanted along with the controller to avoid the need for any external connections to the artificial heart. An inductively coupled battery charger for use outside the recipient's body is positioned proximate the battery charger to provide inductively coupled charging for use in driving the artificial heart.

An apparatus is disclosed including: an intracardiac pump device having a path for a guidewire extending through the pump device from a first opening to a second opening; and a lumen which extends from a first end located outside of the pump device, into the pump device through the first opening in the pump device, along the path for the guidewire, out of the pump device through the second opening, and to a second end located outside of the pump device. The lumen is configured to receive the guidewire such that when the guidewire passes through the lumen from the first end to the second end, the guidewire is positioned along the path.

The invention relates to a pulsatile medical device enabling a blood flow to be circulated including an external pipe presenting an inside wall, an outside wall, and two ends, one end being for connection to an ECC type machine, to a cardiac assistance system or to the patient's body, and one end being for connection to the patient's body; an internal pipe inserted in said external pipe and presenting an inside wall, an outside wall, and two ends fastened all around their peripheries to the external pipe all around its periphery, the blood flow passing through said internal pipe; the outside wall of the internal pipe and the inside wall of the external pipe defining a space for filling with fluid and being connectable via a connector port to an appliance for creating one or more inflations/deflations of said space, thereby creating one or more pulses in the blood flow.

A device to assist the performance of a heart with at least one pump that is formed as a rotary pump and driven via a magneto coupling.

A device to assist the performance of a heart with at least one pump that is formed as a rotary pump and driven via a magneto coupling.

A blood flow conduit includes a first conduit portion defining a first portion of a lumen; and a second conduit portion defining a second portion of a lumen. At least one of the first or second conduit portions may include a tip portion and the other of the first or second conduit portions may include an enlarged area.

The present invention relates to an auxiliary artificial valve for implantation in blood vessel of a mammal patient. The artificial valve is provided with at least a first moving part and a second moving part configured to move between an closed position and an opened position, and a casing comprising at least one hinge, wherein the at least first moving part and second moving part are configured to be movably attached to the casing by means of said at least one hinge. e

The present invention relates to an auxiliary artificial valve for implantation in blood vessel of a mammal patient. The artificial valve is provided with at least a first moving part and a second moving part configured to move between an closed position and an opened position, and a casing comprising at least one hinge, wherein the at least first moving part and second moving part are configured to be movably attached to the casing by means of said at least one hinge. e

Systems and methods are provided for optimizing hemodynamics within a patient's heart, e.g., to improve the patient's exercise capacity. In one embodiment, a system is configured to be implanted in a patient's body to monitor and/or treat the patient that includes at least one sensor configured to provide sensor data that corresponds to a blood pressure within or near the patient's heart; at least one adjustable component designed to cause blood to flow in a direction opposite to the normal direction (regurgitation) within the patient's heart; and a controller configured for adjusting the function of the at least one adjustable component based at least in part on sensor data from the at least one sensor.

An apparatus is disclosed including: an intracardiac pump device having a path for a guidewire extending through the pump device from a first opening to a second opening; and a lumen which extends from a first end located outside of the pump device, into the pump device through the first opening in the pump device, along the path for the guidewire, out of the pump device through the second opening, and to a second end located outside of the pump device. The lumen is configured to receive the guidewire such that when the guidewire passes through the lumen from the first end to the second end, the guidewire is positioned along the path.