A pass-through assembly including a first wall 110d having oppositely-directed inner and outer sides, 112, 114, the first wall 110d defining a first opening 116 extending from the inner side 112 to the outer side 114; an elongated structure 118 extending into the opening 116 from the outer side 114 of the first wall 110d; a first material 130 contacting the first wall 110d and the elongated structure 118 so as to at least partially seal the opening 116, and a second material 140 different from the first material 130, the second material 140 overlying the first material 130 on the outer side 114 of the wall 110d, the second material 140 adhering to the elongated structure 118 and the first wall 110d, the second material 140 having at least one physical property different than a corresponding physical property of the first material 130.

A malleable cannula for fluidically coupling with an anatomical structure includes a flexible cannula body wall having a proximal end, a distal end, and a lumen extending longitudinally between the proximal end and the distal end. The proximal end defines a first opening to the lumen and the distal end defining a second opening to the lumen. A channel is defined by a portion of the cannula body wall and extends longitudinally from the distal end toward the proximal end. The channel has a first end oriented toward the proximal end of the cannula body wall. A malleable member is provided within the channel and is fixedly connected to the cannula body wall at the first end of the channel. The malleable member is configured to assume and maintain a formed shape of the cannula body wall.

Disclosed is an electromechanical device generating bilateral pressure impulses, wherein the alternative and specular movement of the homologous cursors (CV, CO), pacing one of the Cartesian axes, exclusively manages mobile cores (NEM) of electromagnets (EM) with planned solicitation, for supplying the necessary mechanical energy for the correct working of operating machines of different kinds, and in particular of a permanent artificial heart.

A blood pump including a housing defining a fluid flow path, an upstream end, a downstream end, and an outlet at the downstream end. A rotor is disposed within the housing and within the fluid flow path, the rotor being rotatable independent of the housing in a first direction and configured to pump blood downstream toward the outlet. The housing defines an inflow cannula at the upstream end, the inflow cannula defining a proximal end proximate the rotor and an opposite distal end. The inflow cannula defines a major longitudinal axis and minor longitudinal axis, the distal end of inflow cannula defines a plurality of slots radially disposed about the distal end, the plurality of slots being at least one from the group consisting of sloped in the first direction with respect to the major longitudinal axis and angled in the first direction with respect to the minor longitudinal axis.

An apparatus for protecting heart tissue from an implanted inlet element of a blood pump. The apparatus includes a flange member having a first radially constricted configuration and a second radially expanded configuration, the flange member being biased in its second radially expanded configuration. The flange member defines an opening there through sized to receiving the inlet element of the blood pump. A retaining element extending from the flange member is included, the retaining element being flexible and sized to be disposed about at least a portion of the inlet element.

A blood pump including a housing defining a proximal end, a distal end, and a first axis extending from the proximal end to the distal end. A ferromagnetic rotor is disposed within the housing and configured pump blood in a direction along the first axis. A stator is disposed within housing and around the ferromagnetic rotor, the stator is configured to apply a magnetic force causing rotation of the ferromagnetic rotor, the stator being eccentric to the rotor.

A rotary blood pump includes a casing defining a pumping chamber. The pumping chamber has a blood inlet and a tangential blood outlet. One or more motor stators are provided outside of the pumping chamber. A rotatable impeller is within the pumping chamber and is adapted to cause blood entering the pumping chamber to move to the blood outlet. The impeller has one or more magnetic regions. The impeller is radially constrained in rotation by magnetic coupling to one or more motor stators and is axially constrained in rotation by one or more hydrodynamic thrust bearing surfaces on the impeller.

A rotordynamic pump for delivering continuous flow of fluids, such as blood, is provided. In one embodiment, the pump includes a stator housing having an inlet and an outlet. A rotor hub is disposed within the stator housing having a first, mixed-stage impeller and a second, axial-flow stage impellers. One or more stator vanes and extend radially inwardly from the stator housing. In one particular embodiment, the second stage impeller is disposed nearer to the outlet than to the inlet. The stator vanes may include a first set of stator vanes disposed between the first and second stage impellers, and a second set of stator vanes positioned between the second stage impellers and the outlet.

A pumping system (200) for controlling the flow of interatrial blood comprises, housed inside a container (201), a control element (30, 30′, 30″) of the interatrial blood flow. The control element comprises: at least one worm screw (31), the rotation of which creates a two-way flow of interatrial blood; or a pair of counter-rotating propellers (31′); or a pair of membranes (31″) whose deformation creates a two-way flow of interatrial blood; or a flexible structure (31″) whose change in volume within the container (201) creates a two-way flow of interatrial blood.

Improved systems and methods for extracorporeal blood temperature control and patient temperature control, e.g., for induced hypothermia and optional normothermia, may include or otherwise employ a heat exchanger for cooling/warming of a fluid, a thermal exchange module having fluidly isolated first and second volumes, and a fluid pump for circulating the fluid through the heat exchanger and the first volume of the thermal exchange module. A blood pump may be provided for the flow of blood through the second volume of the thermal exchange module, and a first controller may be provided for providing output signals for use in operation of the heat exchanger to selectively control thermal exchange between the fluid circulated through the first volume of the thermal exchange module and the blood flowed through the second volume of the thermal exchange module, thereby providing for selective cooling/warming of the blood. A multi lumen catheter may be utilized for the flow of blood from a patient vascular system to the second volume of the thermal exchange module, and for flow of blood from the second volume of the thermal exchange module back to the patient vascular system. The circulated fluid may be optionally circulated through a patient contact pad(s) for contact cooling/warming, wherein patient cooling/warming may be provided in a first mode via blood cooling/warming in the thermal exchange module, and patient cooling/warming may be provided in a second mode via thermal exchange by the contact pad(s).