A disclosed apparatus or method can include or use a non-transluminally implantantable blood pump housing, which can be sized and shaped to be implanted at an aortic valve of a human subject, the pump housing can include: a pump housing cross-sectional profile size that is larger than is passable via a blood vessel of the human subject; and a power connection, configured for being electrically connected to an intravascular lead that is sized and shaped to extend from the pump housing through a subclavian artery of the human subject.

A catheter pump system includes a catheter assembly having a proximal end, a distal end, and an elongate body extending therebetween, the elongate body defining at least an inner lumen; a motor assembly comprising a shaft assembly extending at least partially within the elongate body of the catheter assembly, the shaft assembly configured to rotate about an axis; a flow diverter housing defining a chamber and a fluid pathway through which a proximally-conveyed fluid flows, wherein the shaft assembly extends outward from the chamber into the inner lumen of the elongate body; and a seal mounted to and extending around the shaft assembly, the seal configured to inhibit fluid within the elongate body of the catheter assembly from entering the chamber at least about an outer periphery of the shaft assembly.

A catheter pump system includes a catheter assembly having a proximal end, a distal end, and an elongate body extending therebetween, the elongate body defining at least an inner lumen; a motor assembly comprising a shaft assembly extending at least partially within the elongate body of the catheter assembly, the shaft assembly configured to rotate about an axis; a flow diverter housing defining a chamber and a fluid pathway through which a proximally-conveyed fluid flows, wherein the shaft assembly extends outward from the chamber into the inner lumen of the elongate body; and a seal mounted to and extending around the shaft assembly, the seal configured to inhibit fluid within the elongate body of the catheter assembly from entering the chamber at least about an outer periphery of the shaft assembly.

A pump is provided with a housing and with an upstream inlet and a downstream outlet and a fluid channel with a channel axis, said fluid channel being arranged between the inlet and outlet. A rotor which can be brought into rotation by way of a motor is arranged within the fluid channel. Furthermore, a sensor arrangement is provided which can detect an inclination of the rotation axis of the rotor.

A pump is provided with a housing and with an upstream inlet and a downstream outlet and a fluid channel with a channel axis, said fluid channel being arranged between the inlet and outlet. A rotor which can be brought into rotation by way of a motor is arranged within the fluid channel. Furthermore, a sensor arrangement is provided which can detect an inclination of the rotation axis of the rotor.

A device for pumping blood, includes a housing having a distal end adapted to be coupled to a catheter, a proximal end having an outlet, and a tubular body extending between the distal and proximal ends along an axis. A rotor is rotatably disposed within the housing. A first magnetic bearing is operative to levitate the rotor along the axis within the housing. A second magnetic bearing controls a rotational frequency of the rotor. A third magnetic bearing controls a radial position of the rotor.

A by-pass shunt for use with a bodily fluid pump. The by-pass shunt includes an inflow conduit, an outflow conduit, and an intermediate conduit fluidically coupling the inflow and outflow conduits. A flow restrictor is operably coupled to a portion of the intermediate conduit and is configured to reduce a fluid flow from the outflow conduit, through the intermediate conduit, and into the inflow conduit.

The invention relates to a rotor for a pump, having at least one blade, the rotor being able to be actuated to rotate about an axis of rotation in order to convey a fluid in the axial or radial direction, the rotor being able to be deformed reversibly elastically in the radial direction between a first, radially compressed state and a second, radially expanded state which the rotor adopts without the effect of external forces, and a third state of the rotor being provided in which, in pumping operation under fluid loading, the rotor is deformed from the first state to beyond the second state.

A cardiac support system can be used to couple a conduit of a pump to a heart. The cardiac support system can include a sewing ring configured for attachment to the heart, a connector having a ring frame attached to the sewing ring, and having a channel and a frame recess extending radially outwardly from the channel and a spring component disposed partially within the frame recess. The cardiac support system can also include a pump housing having a radial protrusion having a distal surface and a proximal surface and a housing recess extending radially inwardly from the radial protrusion and configured to receive a portion of the spring component. The housing may also include a seal to form a fluid tight barrier between the housing and ring frame of the connector.

Apparatus and methods are described including inserting a catheter into a subject's body via a vein of the subject's groin. The catheter is advanced distally such that a distal end of the catheter is disposed inside the subject's renal vein. Respective stabilizing portions of the catheter stabilize the catheter by being in contact with inner walls of, respectively, an iliac vein of the subject, and a vena cava of the subject. Subsequently, a medical device is deployed inside the renal vein by retracting the distal end of the catheter, such that the distal end of the catheter is in a retracted state, in which the respective stabilizing portions of the catheter still stabilize the catheter by being in contact with the inner walls of, respectively, the subject's iliac vein and the subject's vena cava. Other applications are also described.