A pump intended to be immersed in a fluid, including a housing, a brushless motor unit formed by a stator in which first magnetic elements are disposed, a rotor having second magnetic elements intended for magnetic coupling with the first magnetic elements of the stator, a transmission shaft connected to the rotor and constituting, in its upper part, a turbine, the turbine includes, at its apex, an output pivot interacting with a guide fastened to the housing, the guide having a complementary shape to that of the output pivot so as to keep the output pivot stable in rotation and to form a space between the output pivot and the guide, and the guide includes a central opening in the axis of rotation of the output pivot for a passage of fluid from the inside of the housing to the outside via the space and the opening.

Disclosed herein is an inflow cannula for an implantable blood pump assembly. The inflow cannula includes a tubular body that extends from a proximal end to a distal end. The tubular body includes a proximal portion adapted for connection to a pump housing, and a distal portion adapted for positioning within an opening formed in a heart. The inflow cannula further includes an expandable sleeve coupled to an exterior surface of the distal portion. The sleeve has a first portion coupled to the distal portion of the tubular body, and a second portion extending from the distal end of the tubular body. The second portion is deployable from a first, stored configuration to a second, deployed configuration in which the second portion expands radially to engage and conform to an endocardial surface of the heart.

A blood flow assist system can include an impeller assembly including an impeller shaft and an impeller on the impeller shaft, a primary flow pathway disposed along an exterior surface of the impeller. The system can include a rotor assembly at a proximal portion of the impeller shaft. A secondary flow pathway can be disposed along a lumen of the impeller shaft. During operation of the blood flow assist system, blood can be pumped proximally along the primary flow pathway and the secondary flow pathway. The system can include a sleeve bearing distal the impeller. The system can include a drive unit having a distal end disposed distal a proximal end of the second impeller. The drive unit comprising a drive magnet and a drive bearing between the drive magnet and the impeller assembly.

The catheter device comprises a motor at the proximal end of the catheter device and a drive shaft, extending from the proximal end section to the distal end section of the catheter device, for driving a rotating element located at the distal end of the catheter device. The catheter device also comprises a hose-like catheter body which encompasses the drive shaft and extends from the proximal end section to the distal end section. At the proximal end of the catheter device, the drive shaft is connected to a motor by a clutch. The clutch is a magnetic clutch with a proximal and a distal magnet unit. The proximal magnet unit is connected to the motor and the distal magnet unit to the drive shaft. The distal magnet unit is mounted fluid-tight in a clutch housing. The proximal end of the catheter body makes a fluid-tight connection with the clutch housing.

The catheter device comprises a motor at the proximal end of the catheter device and a drive shaft, extending from the proximal end section to the distal end section of the catheter device, for driving a rotating element located at the distal end of the catheter device. The catheter device also comprises a hose-like catheter body which encompasses the drive shaft and extends from the proximal end section to the distal end section. At the proximal end of the catheter device, the drive shaft is connected to a motor by a clutch. The clutch is a magnetic clutch with a proximal and a distal magnet unit. The proximal magnet unit is connected to the motor and the distal magnet unit to the drive shaft. The distal magnet unit is mounted fluid-tight in a clutch housing. The proximal end of the catheter body makes a fluid-tight connection with the clutch housing.

A blood pump having a housing including an inlet element. The inlet element has a proximal portion sized to be received within at least a portion of a heart of a patient and defines a major longitudinal axis. A rotor is configured to rotate within the housing about the major longitudinal axis and impel blood from heart. At least one stator is disposed within the housing and positioned within the housing at least one from the group consisting of upstream and downstream from the rotor. During operation of the blood pump the rotor is maintained at an oblique angle with respect to the major longitudinal axis.

A method of controlling a blood pump including executing a control command to temporarily displace an impeller of the blood pump within a pump housing from a first axial position relative to the pump housing to a second axial position a distance away from the first axial position using a vector control method, and causing the impeller to move from the second axial position to a third axial position, the third axial position including a positive and a negative displacement of the impeller relative to the first axial position.

A heart pump including: a housing forming a cavity including: at least one inlet aligned with an axis of the cavity; and, at least one outlet provided in a circumferential outer wall of the cavity; an impeller provided within the cavity, the impeller including vanes for urging fluid from the inlet to the outlet; and, a drive for rotating the impeller in the cavity and wherein a flow path through the pump has a minimal cross-sectional area of at least 50 mm.sup.2.

A method is provided for producing a bearing arrangement for an implantable blood pump. A bearing arrangement and an implantable blood pump are also provided. In the method, a rotor may be provided having one or more drive magnets. The rotor has a conveying element. In addition, a stator having stator windings is provided. Furthermore, the rotor is arranged in a flow channel formed by an inside wall of the stator. A rotor rotation is then driven. While the rotor rotation is driven, a deflection of the rotor is determined. In addition, the deflection of the rotor may be corrected by applying, removing, magnetizing and/or demagnetizing magnetically active material on the stator and/or on the rotor in a non-rotationally symmetrical manner.

A method is provided for producing a bearing arrangement for an implantable blood pump. A bearing arrangement and an implantable blood pump are also provided. In the method, a rotor may be provided having one or more drive magnets. The rotor has a conveying element. In addition, a stator having stator windings is provided. Furthermore, the rotor is arranged in a flow channel formed by an inside wall of the stator. A rotor rotation is then driven. While the rotor rotation is driven, a deflection of the rotor is determined. In addition, the deflection of the rotor may be corrected by applying, removing, magnetizing and/or demagnetizing magnetically active material on the stator and/or on the rotor in a non-rotationally symmetrical manner.