An implantable pump system is provided, including an implantable blood pump suitable for use as a partial support assist device, the system further including 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 electromagnetic actuator including a magnetic assembly and electromagnetic assembly, so that when the electromagnetic assembly is energized, the electromagnetic assembly causes wavelike undulations to propagate along the flexible membrane to propel blood 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.

A pumping device includes a single-use device and a reusable device. The single-use device is to be inserted into the reusable device and includes two pump units in series, one behind the other. Each pump unit includes a rotor for a bearingless motor, and can be magnetically levitated and driven without contact for rotation about an axial direction. The reusable device includes a stator for each rotor which form an electromagnetic rotary drive for rotating the rotor about the axial direction. Each stator is a bearing and drive stator with which the rotor can be magnetically driven and levitated without contact with respect to the stator. An independent control device is provided for each stator, and can independently activate a respective stator.

The present invention provides an implantable cardiac compression device comprising: an inflatable cardiac compression jacket configured when inflated to directly compress a heart and assist in displacing blood therefrom, a channel that connects the inflatable cardiac compression jacket and an expandable fluid reservoir configured to contain a fluid when displaced compresses the inflatable cardiac compression jacket, and a fluid driver operably connected to the inflatable cardiac compression jacket and to the expandable fluid reservoir, wherein the fluid driver is configured to inflate the cardiac compression jacket and to deflate the expandable fluid reservoir during systole of the heart; said driver is further configured to deflate the cardiac compression jacket and to inflate the expandable fluid reservoir during diastole of the heart.

This centrifugal blood pump apparatus includes an impeller (10) provided in a blood chamber (7), and a plurality of coils (20) provided in a motor chamber (8) for driving the impeller (10) to rotate with a dividing wall (6) interposed therebetween. A flexible substrate (23) in the shape of a strip is arranged to surround outer circumferences of the plurality of coils (20), and is connected to the plurality of coils (20) and a connector (24). A driving voltage (VU, VV, VW) is externally supplied to the plurality of coils (20) via the connector (24) and the flexible substrate (23). Thus, assembling workability, productivity and reliability are improved.

An implantable blood pump includes a control unit storing patient specific settings. The control unit is configured to store patient specific settings. The patient specific settings can be used to determine a target operating speed for the blood pump and/or a target operating mode for the blood pump. The patient specific settings can include at least one of an operating mode for the pump, a set speed for the pump, a lower speed limit for the pump, a patient hematocrit value, a patient hematocrit date, a patient blood density, and a periodic log rate for event and periodic data.

Systems, devices, and methods for improving wireless power transmission are disclosed herein. A method of powering an implantable ventricular assist device with an external charging device includes receiving a signal indicative of a change in a property of a deformable coil of the resonant circuit. A performance property of the deformable coil is determined based on the signal. An adjustment to a tuning of the resonant circuit is identified based on the performance property of the deformable coil. The resonant circuit is tuned according to the adjustment to the tuning of the resonant circuit. The resonant circuit is driven to transmit power to a secondary coil electrically coupled with the implantable ventricular assist device to power the ventricular assist device.

Systems, devices, and methods for improving wireless power transmission are disclosed herein. A method of powering an implantable ventricular assist device with an external charging device includes receiving a signal indicative of a change in a property of a deformable coil of the resonant circuit. A performance property of the deformable coil is determined based on the signal. An adjustment to a tuning of the resonant circuit is identified based on the performance property of the deformable coil. The resonant circuit is tuned according to the adjustment to the tuning of the resonant circuit. The resonant circuit is driven to transmit power to a secondary coil electrically coupled with the implantable ventricular assist device to power the ventricular assist device.

Disclosed herein is an implantable blood pump assembly that includes a housing defining an inlet, an outlet, a flow path extending from the inlet to the outlet, and an internal compartment separated from the flow path. The blood pump assembly further includes a rotor positioned within the flow path and operable to pump blood from the inlet to the outlet, a stator positioned within the internal compartment and operable to drive the rotor, and an inlet conduit connected to the housing inlet and having a downstream end that has a reduced cross-sectional area that produces a localized region of high velocity blood flow. The blood pump assembly further includes at least one pressure sensor positioned between the inlet and the outlet and configured to detect a pressure of blood flowing through the flow path. The pressure sensor is located adjacent the downstream end of the inlet conduit.

Disclosed herein is an implantable blood pump assembly that includes a housing defining an inlet, an outlet, a flow path extending from the inlet to the outlet, and an internal compartment separated from the flow path. The blood pump assembly further includes a rotor positioned within the flow path and operable to pump blood from the inlet to the outlet, a stator positioned within the internal compartment and operable to drive the rotor, and an inlet conduit connected to the housing inlet and having a downstream end that has a reduced cross-sectional area that produces a localized region of high velocity blood flow. The blood pump assembly further includes at least one pressure sensor positioned between the inlet and the outlet and configured to detect a pressure of blood flowing through the flow path. The pressure sensor is located adjacent the downstream end of the inlet conduit.

Integral artificial heart device capable of storing venous blood in dynamic atria, without interrupting the continuous return of the blood. The device comprises a right ventricle (A1) and left ventricle (A2) pulsing simultaneously, and the reactive right atrium (C1) and left atrium (not illustrated) thereof, immersed in a pneumatic spec (D) having a variable vacuum D, which is driven by a solenoid (35), acting sequentially, by repulsion, on the permanent magnet discs (20, 21) included in the elastic ventricular membranes (18, 19), which beat simultaneously in the ventricular spaces (A1) and (A2), and, in the opposite direction, in pneumatic space (D) which houses elastic tubes acting as atria. The device simultaneously ejects systolic volumes, and accepts the proportion of continuously returning venous blood to store in the atria, during the systole, such that said continuous return is not interrupted by sequential systolic closure of the intake ports.