A percutaneous lead assembly for an active implantable device, the lead assembly comprising a sheath with a plurality of wires extending from a proximal end to a distal end. The wires being adapted to power the active implantable device; the distal end having at least one electrode fixed thereon. The electrodes being in communication with sensor electronics and wherein at least one electrode is on the outer layer of the lead assembly in which the electrode is used to detect at least one of acceleration and electrical signals of an organ.

A blood pump device comprising: a centrifugal blood pump having: a pump housing defining an inlet to receive blood and direct blood onto an impeller, the pump housing having a top bezel and a central column directed into the middle of a cavity within the pump housing; the impeller is adapted, in use, to rotate in the cavity around the central column and to be suspended on a pivot bearing mounted between the middle of the lower surface of the impeller and the middle of the upper surface of the central column; the impeller is stabilised, in use, by the rotation of blades generating a centrifugal force acting on the blades in radial direction away from the central column.

A medical device includes a constant-flow pump configured to pump a fluid through a fluid conduit and a rotary valve fluidically connected to the pump. The rotary valve includes at least one rotatable valve member configured to be operatively connected to and rotate relative to the fluid conduit. The rotatable valve member includes at least one aperture. The rotatable valve member is capable of being positioned in a plurality of positions relative to the conduit. The position of the at least one first aperture of the rotatable valve member controls fluid flow through the rotary valve, and thereby through the conduit.

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.

A device for reducing pressure within a lumen includes a reservoir structured for holding a fluid therein, an injection port in fluid communication with the reservoir, a compliant body structured to expand and contract upon changes in pressure, and a conduit extending between and fluidly coupling the reservoir and the compliant body. The fluid may be a compressible or a noncompressible fluid.

A catheter pump system with a pump having a fluid displacement member in the blood flow channel, a motor and a motor controller having a pressure sensing port for connection to a control pressure source. The motor controller is arranged for causing motor speed to be increased in response to a reduction of pressure applied to the pressure sensing port and for causing motor speed to be reduced in response to an increase of pressure applied to the pressure sensing port. The motor may be a pneumatic motor for driving the pump and the motor controller may be arranged for controlling motor speed by reducing flow through a supply channel to the motor and allowing an increase of flow through the supply channel to the motor in response to control signals received via an input interface.

A catheter pump system with a pump having a fluid displacement member in the blood flow channel, a motor and a motor controller having a pressure sensing port for connection to a control pressure source. The motor controller is arranged for causing motor speed to be increased in response to a reduction of pressure applied to the pressure sensing port and for causing motor speed to be reduced in response to an increase of pressure applied to the pressure sensing port. The motor may be a pneumatic motor for driving the pump and the motor controller may be arranged for controlling motor speed by reducing flow through a supply channel to the motor and allowing an increase of flow through the supply channel to the motor in response to control signals received via an input interface.

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.

Methods for synchronizing the actions of a pulsatile cardiac assist device with a dysfunctional heart using a cardiac pacemaker. Aspects include receiving a signal from the pacemaker and actuating the pulsatile cardiac assist device in response to the signal from the pacemaker to either help push blood out of the heart during systole or to help suck blood from the atria during diastole.

A cardiac assist device including a sleeve configured to externally wrap around a native, intact heart; a motor, and a drive shaft that connects the motor to the sleeve, wherein, actuation of the motor and the drive shaft provides a synchronized assisting force to a pumping force of the native, intact whole heart, thereby helping contraction and expansion of the heart located within an internal volume defined by the sleeve. Some embodiments relate to a system for synchronizing the cardiac assist device with a heart including the cardiac assist device; a power supply connected to the motor; and an electrical connector-relay configured to receive electrical signals from the pacemaker and to generate actuating signals that are relayed to the motor and the drive shaft, wherein, during operation of the system in a subject, the heart is assisted in contracting synchronously with the pacemaker signal rhythm.