Multi-cell battery packs can be made safer with certain features that mitigate the consequences of cell failure. Parameters of a cell are monitored to determine when the cell should be disconnected from the pack in case of a fault. The battery is reconfigured to continue operating in a safer mode. An over-charging prevention system reduces the maximum voltage that remaining battery pack can be charged to, so that the cells do not overcharge. Additional circuitry allows the disconnected cell to be periodically reconnected to the battery pack to determine if its conditions have sufficiently improved. The cells also include components for self-powering these cell functions while it is disconnected from the rest of the circuit.

A minimally invasive system for a wireless circulatory support pump that utilizes a low profile catheter-based techniques and provides temporary and chronic circulatory support depending on the needs of the subject. The system includes a wireless circulatory assist pump, a deployment catheter, and a retrieval catheter for inserting and removing the wireless circulatory assist pump from a subject. The wireless circulatory support pump is relatively easy to place, has high flow rates, and provide improvements in the subject's renal function.

A minimally invasive system for a wireless circulatory support pump that utilizes a low profile catheter-based techniques and provides temporary and chronic circulatory support depending on the needs of the subject. The system includes a wireless circulatory assist pump, a deployment catheter, and a retrieval catheter for inserting and removing the wireless circulatory assist pump from a subject. The wireless circulatory support pump is relatively easy to place, has high flow rates, and provide improvements in the subject's renal function.

The invention relates to a device (10) for inductive energy transmission into a human body (1), having a transmitter coil (24) and/or a receiver coil (14) having a first magnetic core (26) and a resonance or choke coil (16, 34) having a second magnetic core (32), wherein the first magnetic core (26) forms a part of the second magnetic core (32).

The invention relates to a device (10) for inductive energy transmission into a human body (1), having a transmitter coil (24) and/or a receiver coil (14) having a first magnetic core (26) and a resonance or choke coil (16, 34) having a second magnetic core (32), wherein the first magnetic core (26) forms a part of the second magnetic core (32).

Disclosed herein is an outflow graft assembly for an implantable blood pump. The outflow graft assembly includes a graft, a locking nut including a plurality of planar edges and a plurality of corners, and a U-shaped fixation clip. The U-shaped fixation clip includes a first flat segment including a first flexure including a first locking feature, a second flat segment including a second flexure including a second locking feature, an arcuate segment extending between the first flat segment and the second flat segment, and a lip including a first flat and a second flat. The U-shaped fixation clip is configured to engage the locking nut such that the first and second locking features contact associated corners of the plurality of corners and the first and second flats contact associated planar edges of the plurality of planar edges, thereby preventing rotation of the locking nut relative to the fixation clip.

Apparatus is provided for treating heart failure, the apparatus including one or more propeller blades and a controller, which is configured to rotate the one or more propeller blades to produce continuous non-pulsatile blood flow not synchronized with a cardiac cycle of a subject. An intra-atrial anchor includes a stent surrounding the one or more propeller blades. The intra-atrial anchor is coupled to the one or more propeller blades and configured to be anchored in a left atrium of the subject so as to position the one or more propeller blades in the left atrium oriented such that the one or more propeller blades, when rotated by the controller, draw blood from the left atrium and expel the blood in the left atrium toward a mitral valve, thereby increasing atrial pressure above the mitral valve. Other embodiments are also described.

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. Alternatively, the sensor monitors the heart based on admittance while the cardiac assist device. Alternatively, the sensor monitors the heart based on impedance.

An implantable right ventricular assist device configured to be implanted within the right ventricle of a heart, including a percutaneously deliverable centrifugal pump configured to carry the blood from the right ventricle to the pulmonary artery; an exit cylinder configured to secure directly or indirectly the centrifugal pump within a portion of the pulmonary artery; and a power source. Also, a method to percutaneously and transluminally implant the right ventricular assist device within the right ventricle of a patient's heart. Further, the use of the right ventricular assist device to long-term assist of the right ventricle of a patient's heart.

An implantable right ventricular assist device configured to be implanted within the right ventricle of a heart, including a percutaneously deliverable centrifugal pump configured to carry the blood from the right ventricle to the pulmonary artery; an exit cylinder configured to secure directly or indirectly the centrifugal pump within a portion of the pulmonary artery; and a power source. Also, a method to percutaneously and transluminally implant the right ventricular assist device within the right ventricle of a patient's heart. Further, the use of the right ventricular assist device to long-term assist of the right ventricle of a patient's heart.