Provided is a blood pump controller capable of preventing an operation error in performing a battery exchange with a small-sized and light-weighted configuration and exhibiting high waterproof property. A blood pump controller includes: a controller body for driving a blood pump; a battery pack having a first surface on which an electricity-supply-side battery connection connector is disposed and supplying stored electricity to the controller body; and a battery housing body having a slot which has a second surface on which an electricity-receiving-side battery connection connector is disposed and in which the battery pack is housed and held. When the battery pack is housed in the slot, an electrical connection is made between a pair of the battery connection connectors, the first surface and the second surface opposedly face each other, and a first sealing member provides sealing such that the first sealing member surrounds the pair of battery connection connectors.

Provided is a blood pump controller capable of preventing an operation error in performing a battery exchange with a small-sized and light-weighted configuration and exhibiting high waterproof property. A blood pump controller includes: a controller body for driving a blood pump; a battery pack having a first surface on which an electricity-supply-side battery connection connector is disposed and supplying stored electricity to the controller body; and a battery housing body having a slot which has a second surface on which an electricity-receiving-side battery connection connector is disposed and in which the battery pack is housed and held. When the battery pack is housed in the slot, an electrical connection is made between a pair of the battery connection connectors, the first surface and the second surface opposedly face each other, and a first sealing member provides sealing such that the first sealing member surrounds the pair of battery connection connectors.

A medical device for anchoring a cardiac pump in an opening of a ventricular wall of a heart, including a connector to be fitted to the ventricular wall. The connector includes a connection flange and a support skirt. The skirt is to be placed outside the heart when the flange is joined to the ventricular wall. The connector defines a first opening for a part of the body of an insert to pass through. The insert is rigid and defines a second opening for the body of the pump to pass through. The insert includes a distal end that is to be placed inside the heart and a proximal end that is to be placed outside the heart when the insert is joined to the connector. At least one element locks/unlocks the insert in position with respect to the connector when the insert has been introduced into the connector.

A medical device for anchoring a cardiac pump in an opening of a ventricular wall of a heart, including a connector to be fitted to the ventricular wall. The connector includes a connection flange and a support skirt. The skirt is to be placed outside the heart when the flange is joined to the ventricular wall. The connector defines a first opening for a part of the body of an insert to pass through. The insert is rigid and defines a second opening for the body of the pump to pass through. The insert includes a distal end that is to be placed inside the heart and a proximal end that is to be placed outside the heart when the insert is joined to the connector. At least one element locks/unlocks the insert in position with respect to the connector when the insert has been introduced into the connector.

A heart support system is provided includes a control unit and sound-generating devices, said control unit configured to detect and process alarm events and to carry out control tasks in the heart support system. The heart support system further includes a storage device configured to store one or more defined alarm signal time curves and one or more alarm priorities. Each alarm signal time curve and each alarm priority is assigned to an alarm event. A sound-generation controller is configured such that when an alarm event is detected, the controller overlays a volume time curve onto the alarm signal time curve assigned to the alarm event in the storage device, said volume time curve based on the alarm priority assigned to the respective alarm event in the storage device and the length of time since the detection of the alarm event.

A pump system is provided comprising a diaphragm fluid pump which can be fluidically connected to a heart and/or at least one blood vessel by means of an inlet cannula and an outlet cannula and is adapted for generating a pulsatile fluid flow for supporting a cardiac activity of the heart, a working pressure source connected to the diaphragm fluid pump by means of a pressure line and adapted for providing a working pressure for driving the diaphragm fluid pump, a control unit adapted for controlling the working pressure, a first flow sensor adapted for detecting a first cannula flow signal corresponding to an inlet flow in the inlet cannula or an outlet flow in the outlet cannula, a working pressure sensor adapted for detecting a working pressure signal corresponding to the working pressure in the pressure line.

An inlet cannula is provided for supplying a fluid from a human vessel to a fluid pump, the inlet cannula formed as a hollow structure suitable for conveying the fluid and a surface of the inlet cannula has an ingrowth zone and an inlet zone separated from each other by a tear-off edge extending in the circumferential direction of the inlet cannula, wherein a first tangent to the inlet zone on the tear-off edge has an angle to a longitudinal axis of the inlet cannula of >0° and <180°, and wherein a surface roughness in the ingrowth zone is greater than a surface roughness in the inlet zone, and wherein along the flow direction the ingrowth zone is concave, convex, or not curved and the inlet zone is convexly curved, and wherein the tear-off edge forms a curvature transition between the ingrowth zone and the inlet zone.

An inlet cannula is provided for supplying a fluid from a human vessel to a fluid pump, the inlet cannula formed as a hollow structure suitable for conveying the fluid and a surface of the inlet cannula has an ingrowth zone and an inlet zone separated from each other by a tear-off edge extending in the circumferential direction of the inlet cannula, wherein a first tangent to the inlet zone on the tear-off edge has an angle to a longitudinal axis of the inlet cannula of >0° and <180°, and wherein a surface roughness in the ingrowth zone is greater than a surface roughness in the inlet zone, and wherein along the flow direction the ingrowth zone is concave, convex, or not curved and the inlet zone is convexly curved, and wherein the tear-off edge forms a curvature transition between the ingrowth zone and the inlet zone.

The present invention is generally related to methods and systems for preventing onset or worsening of RHF in patients with implanted ventricular assist devices. More particularly, the present invention relates to identifying patients at risk for RHF following implantation of a ventricular assist device based on pulmonary artery pressure measurement and/or trends and adjusting a pump operating parameter to prevent or reduce the onset or worsening of RHF in such patients, improve patient outcomes, or reduce mortality risks associated with VAD implantation. In particular, a pump operating parameter may be adjusted to reduce or minimize particularly high pressure loads on a patient's heart or amount of time the patient is exposed to such high pressure loads following implantation.

The invention generally relates to improved medical blood pump devices, systems, and methods. For example, blood pumps may be provided that include a housing defining a blood flow path between an inlet and an outlet. A rotor may be positioned in the blood flow path. A motor stator may be driven to rotate the rotor to provide the blood flow through the pump. Axial and/or tilt stabilization components may be provided to increase an axial and/or tilt stabilization of the rotor within the blood flow path. In some embodiments, biasing forces are provided that urge the rotor toward a bearing component. The biasing force may be provided by adjusting drive signals of the motor stator. Additionally, or alternatively, one or more magnets (e.g., permanent/stator magnets) may be provided to bias the rotor in the upstream and/or downstream direction (e.g., toward a bearing (chamfer, step, conical), or the like).