An intravascular blood pump having a rotatable shaft carrying an impeller and a housing with an opening through which the shaft extends with the impeller positioned outside the housing. The shaft and the housing have surfaces forming a circumferential gap which converges towards the impeller-side end of the gap and which has a minimum gap width of preferably no more than 5 μm, more preferably no more than 2 μm.

An intravascular blood pump having a rotatable shaft carrying an impeller and a housing with an opening through which the shaft extends with the impeller positioned outside the housing. The shaft and the housing have surfaces forming a circumferential gap which converges towards the impeller-side end of the gap and which has a minimum gap width of preferably no more than 5 μm, more preferably no more than 2 μm.

A method of controlling an implantable blood pump including a housing having a proximal portion including an inlet, a distal portion including an outlet, and an impeller therein, the method including detecting when a pressure in the housing exceeds a pressure threshold and executing a first vector control command to displace the impeller axially in a distal direction from a primary position to a secondary position different than the primary position in response to the pressure exceeding the pressure threshold.

Blood pump devices having improved rotary seals for sealing a bearing assembly supporting a rotor provided herein. Such rotary seals are particularly suited for use in blood pump devices that include rotors having cantilevered supported through a sealed mechanical bearing disposed outside a blood flow path of the device to avoid thrombus formation caused by blood contact with the bearing. The rotary seal can include a first and second face seal that are preloaded with a deflectable compliance member incorporated into the pump housing or a pair of magnets. Such rotary seals can instead or further utilize tight fitment between components or a bio-absorbable fill material to seal an interface between the rotor shaft and pump housing to seal the bearing assembly from fluid flowing through the pump.

A fluid pump for conveying a fluid is provided comprising: a housing with a fluid inlet and a fluid outlet, a rotor which is disposed rotatably about an axis of rotation in the housing, and a rotor body and at least one conveying element connected rigidly to the rotor body in order to convey the fluid from the fluid inlet to the fluid outlet, the rotor being mounted in the housing radially to the axis of rotation by means of a passive magnetic bearing and also axially and radially by means of a mechanical and/or hydrodynamic bearing disposed on the inlet side or outlet side. A safety bearing is disposed on one side of the rotor situated opposite the mechanical and/or hydrodynamic bearing, wherein the safety bearing has a first safety bearing component connected rigidly to the rotor and a second safety bearing component connected rigidly to the housing.

A controller for an implantable blood pump, having processing circuitry configured to control an operating speed of an impeller of the implantable blood pump. The processing circuitry being further configured to control activation and deactivation of a sleep mode. During the sleep mode the processing circuitry being configured to measure a level of suction by detecting suction during a predetermined time interval, recording the time at which suction occurred during the predetermined time interval, and generating a graph demonstrating the measured level of suction. The measured level of suction being a percentage of time the implantable blood pump experienced suction during the predetermined time interval. The processing circuitry being configured to reduce the operating speed of the impeller if the measured level of suction exceeds a predetermined threshold.

An implantable blood pump including an impeller, at least a portion of the impeller being composed of a metal alloy that is a solid at normal body temperature and is configured to phase change to a liquid between a predetermined temperature above normal body temperature and about 40 degrees Celsius.

A blood pump including a housing having an inflow tube defining a major axis spanning through the inflow tube and a flow path spanning along the major axis, a rotor disposed within the inflow tube, the rotor and the inflow tube defining a gap therebetween, a stator surrounding the inflow tube and the rotor, and the housing defining an access conduit spanning through the inflow tube and the stator transverse to the major axis, the access conduit being in communication with the gap.

A method of determining a cumulative presence of suction in a patient having an implanted blood pump including determining whether at least one suction event occurred during a predetermined time interval for a predetermined number of time intervals and determining the cumulative presence of suction by dividing a sum of a number of predetermined time intervals in which at least one suction event occurred by the predetermined number of time intervals.

A fluid pump for conveying a fluid is provided comprising: a housing with a fluid inlet and a fluid outlet, a rotor which is disposed rotatably about an axis of rotation in the housing, and a rotor body and at least one conveying element connected rigidly to the rotor body in order to convey the fluid from the fluid inlet to the fluid outlet, the rotor being mounted in the housing radially to the axis of rotation by means of a passive magnetic bearing and also axially and radially by means of a mechanical and/or hydrodynamic bearing disposed on the inlet side or outlet side. A safety bearing is disposed on one side of the rotor situated opposite the mechanical and/or hydrodynamic bearing, wherein the safety bearing has a first safety bearing component connected rigidly to the rotor and a second safety bearing component connected rigidly to the housing.