A rotary pump housing having a cylindrical bore, a pumping chamber and a motor stator including an electrically conductive coil located within the housing and surrounding a portion of the cylindrical bore. A rotor has a cylindrical shaft with an impeller and one or of magnets located within the shaft that are responsive to the motor stator to drive actuation of the rotor. The housing bore is closely fitted to the outer surface of the shaft forming a hydrodynamic journal bearing with an annular clearance defining a leakage flow path. One or more of radial or axial thrust bearings may be provided to provide rotation stability to the rotor and flow within the leakage flow path. The relative orientation of positions of the inflow, outflow, and leakage flow paths may be varied within the pump, such as to accommodate different intended methods for implantation and/or use.

Mechanical circulatory supports configured to operate in series with the native heart are disclosed. In an embodiment, a centrifugal pump is used. In an embodiment, inlet and outlet ports are connected into the aorta and blood flow is diverted through a lumen and a centrifugal pump between the inlet and outlet ports. The supports may create a pressure rise between about 40-80 mmHg, and maintain a flow rate of about 5 L/min. The support may be configured to be inserted in a collinear manner with the descending aorta. The support may be optimized to replicate naturally occurring vortex formation within the aorta. Diffusers of different dimensions and configurations, such as helical configuration, and/or the orientation of installation may be used to optimize vortex formation. The support may use an impeller which is electromagnetically suspended, stabilized, and rotated to pump blood.

Mechanical circulatory supports configured to operate in series with the native heart are disclosed. In an embodiment, a centrifugal pump is used. In an embodiment, inlet and outlet ports are connected into the aorta and blood flow is diverted through a lumen and a centrifugal pump between the inlet and outlet ports. The supports may create a pressure rise between about 40-80 mmHg, and maintain a flow rate of about 5 L/min. The support may be configured to be inserted in a collinear manner with the descending aorta. The support may be optimized to replicate naturally occurring vortex formation within the aorta. Diffusers of different dimensions and configurations, such as helical configuration, and/or the orientation of installation may be used to optimize vortex formation. The support may use an impeller which is electromagnetically suspended, stabilized, and rotated to pump blood.

The invention relates to a device (10) for inductive energy transmission into a human body (1), having a transmitter coil (24) and/or a receiver coil (14) having a first magnetic core (26) and a resonance or choke coil (16, 34) having a second magnetic core (32), wherein the first magnetic core (26) forms a part of the second magnetic core (32).

The invention relates to a device (10) for inductive energy transmission into a human body (1), having a transmitter coil (24) and/or a receiver coil (14) having a first magnetic core (26) and a resonance or choke coil (16, 34) having a second magnetic core (32), wherein the first magnetic core (26) forms a part of the second magnetic core (32).

The present invention relates to provides a heart assist device comprising one or more blood pumps for connection to a heart, a control module for controlling operation of the one or more pumps, a power module for powering the operation of the control module and the one or more pumps, and a lead for supplying power between the control module and the one or more pumps. The heart assist device includes a control module adapted for controlling operation of one blood pump, in a left ventricular assistance device configuration in or a right ventricular assistance device configuration, or for controlling two blood pumps in a bi-ventricular assistance device configuration.

The present invention relates to provides a heart assist device comprising one or more blood pumps for connection to a heart, a control module for controlling operation of the one or more pumps, a power module for powering the operation of the control module and the one or more pumps, and a lead for supplying power between the control module and the one or more pumps. The heart assist device includes a control module adapted for controlling operation of one blood pump, in a left ventricular assistance device configuration in or a right ventricular assistance device configuration, or for controlling two blood pumps in a bi-ventricular assistance device configuration.

Systems and related methods for supplying power to a medical device employ serially-connectable portable batteries. A method of supplying electrical power to a medical device includes discharging a first external battery to output electrical power to a second external battery. Distribution of the electrical power received by the second external battery is controlled to simultaneously charge the second external battery and output electrical power from the second external battery to supply electrical power to the medical device.

An implantable pump system is provided, suitable for use as a left ventricular assist device (LVAD) system, having an implantable pump, an extracorporeal battery and a controller coupled to the implantable pump, and a programmer selectively periodically coupled to the controller to configure and adjust operating parameters of the implantable pump. The implantable pump includes a flexible membrane coupled to an actuator assembly that is magnetically engagable with electromagnetic coils, so that when the electromagnetic coils are energized, the actuator assembly causes wavelike undulations to propagate along the flexible membrane to propel blood from through the implantable pump. The controller may be programmed by a programmer to operate at frequencies and duty cycles that mimic physiologic flow rates and pulsatility while operating in an efficient manner that avoids thrombus formation, hemolysis and/or platelet activation.

An apparatus includes an expandable member, a blood pump, and a set of struts. The expandable member is configured to transition from a collapsed configuration to an expanded configuration. The expandable member includes a set of flexible segments that form a tubular wall defining an interior volume. The flexible segments contact an inner surface of a blood vessel when the expandable member is in the expanded position. The expandable member includes a set of attachment portions. Each of the struts has a first end portion coupled to a housing of the blood pump. Each of the struts has a second end portion configured to be removably coupled to a corresponding attachment portion such that the blood pump can be removably coupled to the expandable member with at least a portion of the housing disposed within the interior volume of the expandable member.