A pump for mimicking physiological blood flow in a patient is disclosed. The pump works via compression and decompression of a tube, inducing a peristaltic flow within the tube. The compression may be effected by a linear actuator, or alternatively by a pivoting compression member. A one-way check valve ensures flow in a single direction.

A device for extracting arterial and pulmonary embolisms is described herein. The device comprises a suction catheter and a return catheter attached to a reservoir. The reservoir comprises two filters that filter out any unwanted material from the blood. The device may be controlled by a console with a pedal. Blood containing unwanted material is suctioned out of a patient, is filtered in the reservoir, and is returned to the patient. The device prevents blood loss from the patient by returning the blood back to the patient after it is filtered. Furthermore, the filtration system is designed to also remove air from the blood as it is suctioned from the patient.

An electromagnetic rotary drive includes a rotor including a magnetically effective core surrounded by a stator. The stator has poles arranged around the magnetically effective core and each of the poles is delimited by an end face. The rotor is capable of being magnetically driven without contact in an operating state about an axial direction, and is capable of being magnetically levitated without contact with respect to the stator. The rotor is configured to be magnetically levitated in a radial plane and is passively magnetically stabilized in the axial direction against tilting. The magnetically effective core has a rotor height which is a maximum extension of the magnetically effective core in the axial direction, the rotor height being greater than a stator pole height defined by a maximum extension of the end faces in the axial direction.

An electromagnetic rotary drive includes a rotor and a stator. The rotor magnetically driven without contact about an axial direction, and magnetically levitated without contact with respect to the stator. The rotor actively magnetically levitated in a radial plane and passively magnetically stabilized in the axial direction against tilting. The stator has coil cores, each including a longitudinal limb extending in the axial direction and a transverse limb arranged in the radial plane. The transverse limb extends from the longitudinal limb and is bounded by an end face. A concentrated winding is arranged on each of the longitudinal limbs surrounding a respective longitudinal limb. The end faces have a first distance in the radial direction from a first portion and a second distance in the radial direction from a second portion, the second distance greater than the first distance.

An apparatus for a heart of a patient having a cardiac assist device adapted to be implanted into the patient to assist the heart with pumping blood. The apparatus has a sensor adapted to be implanted into the patient. The sensor in communication with the cardiac assist device and the heart which measures native volume of the heart. The apparatus has a first cardiac assist device and a second cardiac assist device tuned to maximize blood flow to the body of the patient, while resting the heart so the heart may recover function. Alternatively, the sensor monitors the heart based on admittance while the cardiac assist device. Alternatively, the sensor monitors the heart based on impedance.

A diaphragm assembly for a pulsatile fluid pump includes an edge-mounted flexible diaphragm, the diaphragm configured for operation cyclically between a diastole mode and a systole mode. The diaphragm assembly further includes a systolic distribution brace having an interior wall configured to cup a portion of the outside surface of the diaphragm, and a diastolic plate, embedded in the diaphragm, mechanically coupled to a portion of the inside surface of the diaphragm. In the course of the systole mode, force is applied across the maximum radial extent of the systolic distribution brace, so as to impart tension in the diaphragm around the periphery of the systolic distribution brace. In the course of the diastole mode, force is applied across the maximum radial extent of the diastolic plate, so as to impart tension in the diaphragm around the diastolic plate.

A diaphragm assembly for a pulsatile fluid pump includes an edge-mounted flexible diaphragm, the diaphragm configured for operation cyclically between a diastole mode and a systole mode. The diaphragm assembly further includes a systolic distribution brace having an interior wall configured to cup a portion of the outside surface of the diaphragm, and a diastolic plate, embedded in the diaphragm, mechanically coupled to a portion of the inside surface of the diaphragm. In the course of the systole mode, force is applied across the maximum radial extent of the systolic distribution brace, so as to impart tension in the diaphragm around the periphery of the systolic distribution brace. In the course of the diastole mode, force is applied across the maximum radial extent of the diastolic plate, so as to impart tension in the diaphragm around the diastolic plate.

A method of manufacturing a medical device including a case having a first and a second case portion mated together. The case having a space inside and an elastic membrane attached to the case. A first housing space covered by the first case portion and a second housing space covered by the second case portion. Fixing parts at peripheries of the first and the second case portions and at which the first and the second case portions are mated. Holding surfaces at the peripheries of the first and the second case portions. A sealing part at the periphery of the first or the second ease portions with respect to the fixing parts and that seals an entirety of the peripheral edge of the elastic membrane. Forming an air gap between the sealing part and the fixing parts by depressurization or heating the fixing parts that connect the case portions.

A controller for a blood pump, in particular a catheter-based intravascular blood pump, configured to utilize detected or determined aortic pressures and left ventricular pressures in order to calculate a coupling factor, which is then used to determine how to adjust the rotational speed of the blood pump, such as when the blood pump is used in conjunction with ECMO devices.

An aspiration system includes a plurality of catheters located at least partially within the lumen of an outer sheath. The outer sheath and the catheters are configured to slide relative to each other between a first state in which the distal ends of the catheters are located within the lumen of the outer sheath, and a second state in which the distal end and an end length section of each catheter is extended through the distal end of the outer sheath and outside of the lumen of the outer sheath. The end length section of each catheter is configured to spring or flare outward relative to the first state, when the outer sheath and the plurality of catheters are in the second state. The distal end of the outer sheath may be placed in an inferior vena cava or iliac vein in a transplant kidney patient, adjacent at least one renal vein, with the outer sheath and the plurality of catheters in the first state. Then, the system may be transitioned to the second state to cause the end length sections of the catheters to spring or flare outward adjacent the renal vein. The catheters are connected to a suction source for aspiration through the catheter end length sections.