A blood pump (10) includes a pump housing (30) having a pump inlet (16) and a pump outlet (18) spaced apart along a longitudinally extending central pump axis (28). The blood pump (10) also includes a rotating assembly (100) comprising an impeller (104). The blood pump (10) further includes partial arc journal bearings (160, 180) that support the rotating assembly (100) for rotation in the housing (30). The rotating assembly (100) is rotatable relative to the housing (30) to pump blood from the pump inlet (16) to the pump outlet (18).

A cardiac pump having a turbine with internal blades, includes a pump designed to circulate a fluid, including a housing, and a turbine which is arranged in the housing and is designed to move rotationally relative to the housing. The turbine includes a body designed to move rotationally, a hollow central part which extends through the body from one side to the other and is intended to allow the fluid to pass through the turbine, and at least one blade that is positioned on the inner wall of the body, in the hollow central part, and is designed to circulate the fluid.

A ventricular assist device for use in a human recipient includes a housing within which a series pair of turbine pump segments and at least one set of deswirlers are operative. The series pair of turbine pump segments provides a redundancy in turn enhances the safety factor provided by the ventricular assist device. 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 ventricular assist device. 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 ventricular assist device.

An inlet tube of a circulatory support device includes a first end configured to receive incoming blood and a second end coupled to a first end of a blood pump. A lumen extends from the first end to the second end, and a spiral feature is disposed within the lumen and configured to support a spiral flow of the incoming blood.

A ventricular assist device for use in a human recipient includes a housing within which a series pair of turbine pump segments, each having a deswirler, are operative. The series pair of turbine pump segments provides a redundancy which in turn enhances the safety factor provided by the ventricular assist device.

An inlet tube of a circulatory support device includes a first end configured to receive incoming blood and a second end coupled to a first end of a blood pump. A lumen extends from the first end to the second end, and a spiral feature is disposed within the lumen and configured to support a spiral flow of the incoming blood.

An inlet tube of a circulatory support device includes a first end configured to receive incoming blood and a second end coupled to a first end of a blood pump. A lumen extends from the first end to the second end, and a spiral feature is disposed within the lumen and configured to support a spiral flow of the incoming blood.

A temporary, removable mechanical circulatory support heart-assist device has at least two propellers or impellers. Each propeller or impeller has a number of blades arranged around an axis of rotation. The blades are configured to pump blood. The two propellers or impellers rotate in opposite directions from each other. The device can be configured to be implanted and removed with minimally invasive surgery.

The invention generally relates to improved medical blood pump devices, systems, and methods. For example, blood pumps may be provided that include a housing defining a blood flow path between an inlet and an outlet. A rotor may be positioned in the blood flow path. A motor stator may be driven to rotate the rotor to provide the blood flow through the pump. Axial and/or tilt stabilization components may be provided to increase an axial and/or tilt stabilization of the rotor within the blood flow path. In some embodiments, biasing forces are provided that urge the rotor toward a bearing component. The biasing force may be provided by adjusting drive signals of the motor stator. Additionally, or alternatively, one or more magnets (e.g., permanent/stator magnets) may be provided to bias the rotor in the upstream and/or downstream direction (e.g., toward a bearing (chamfer, step, conical), or the like).

A connection system for an implantable blood pump including a pump housing having an impeller disposed therein and a motor housing including a motor disposed therein, the motor housing spaced a distance from the pump housing. A flexible outer sheath couples the pump housing to the motor housing, the outer sheath defining a maximum total length between 7 and 10 centimeters. An inner shaft is coaxial with the outer sheath and couples the motor to the impeller.