Abstract: A ventricular assist device includes a pump including a housing having an inlet, an outlet and a moveable element disposed in the housing for urging blood from the inlet to the outlet. An outflow cannula having a proximal end attached to the pump housing, a distal end remote from the pump housing, an interior bore in communication with the outlet of the pump housing, and at least one outlet aperture communicating with the interior bore remote from the pump housing is included. At least one sensor mounted to the outflow cannula and configured to detect a parameter of blood flowing at least one from the group consisting of through the outflow cannula and about an exterior of the outflow cannula is included.

Abstract: 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.

Abstract: A control circuit for monitoring operation of an implantable blood pump, the control circuit operatively couplable to a testing apparatus for simulating blood pump operating conditions and testing the control circuit based on the simulated blood pump operating conditions. The control circuit includes an input module for receiving at least one of one of actual operating data from an implantable blood pump and simulated operating data from the testing apparatus. A processor for processing the received operating data is included, the processor configured to determine a source of the received operating data, and to determine whether the received operating data is actual operating data or simulated operating data based on the determined source.

Abstract: A percutaneous connector assembly including a feedthrough assembly having a body and a plurality of electrically conductive feedthroughs extending through the body from a first end toward a second end thereof. A cable assembly having a plurality of conductors arranged side-by-side within a first plane to form a substantially flat portion thereof is included, each conductor being connected to a corresponding feedthrough of the feedthrough assembly and the flat portion extending from the body.

Abstract: 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.

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

Abstract: The present disclosure provides for a method, control device, and implantable system, for acquiring a plurality of flow rate data points over time, each data point indicative of a flow rate of blood through the pump, calculating, based on the plurality of acquired flow rate data points, a value characterizing one or more features of a waveform formed from the plurality of flow rate data points; and determining, based on the value, the presence or absence of a suction condition in the pump.

Abstract: A pump for a fluid which can be blood has a stator housing and a rotor hub with leading and trailing portions and an intermediate portion disposed therebetween. At least one impeller blade at the leading portion drives circumferential and axial components of a flow into a pump annulus or intermediate pathway portion. At least one stator blade extends radially inward from the stator housing within the intermediate pathway portion and is configured to reduce a circumferential component of the flow.

Abstract: A control circuit includes a pump shutdown module responsive to one or more inputs indicating at least from the group consisting of an operational error at the implantable blood pump and an adverse physiological state of a user of the implantable blood pump. The pump shutdown module ceases operation of the implantable blood pump in response to the one or more inputs. A pump restart module configured to resume operation of the implantable blood pump in response to a first pump restart input and a second pump restart input is included. A pump restart lockout module configured to initiate a pump lockout mode in response to a lockout input is included. The pump lockout mode prevents resumption of operation of the implantable blood pump in response to the first pump restart input and allows resumption of operation of the implantable blood pump in response to the second pump restart input.

Abstract: The present disclosure provides for methods and systems for determining heart rate of a patient. Based on motor current signals of a ventricular assist device (VAD), each of first, second and third events in the measured current signal may be detected, the first event being indicative of a rise or fall in the current signal, the second event being indicative of a rise or fall in the current signal in the opposite direction as the first event, and the third event being indicative of a rise or fall in the current signal in the same direction as the first event. A timer counter may be initiated upon detection of the first event, and an elapsed time may be measured upon detection of the third event. Heart rate may be determined based on the elapsed time of the timer counter.

Abstract: A TET system is operable to vary an amount of power transmitted from an external power supply to an implantable power unit in accordance with a monitored condition of the implantable power unit. The amount of power supplied to the implantable power unit for operating a pump, for example, can be varied in accordance with a cardiac cycle, so as to maintain the monitored condition in the power circuit within a desired range throughout the cardiac cycle.

Abstract: A mechanical circulatory support device. The mechanical circulatory support device includes an inner casing defining a fluid flow path, the fluid flow path defines a longitudinal axis. A rotor is mounted within the fluid flow path and configured to rotate about the longitudinal axis. A housing is included, the inner casing and the rotor being substantially disposed within the housing. The housing having a cross-sectional shape in a plane transverse to the longitudinal axis which decreases in thickness extending from a medial position to opposite lateral positions.

Abstract: A medical device system includes a medical device configured to be carried by a patient and a plurality of controllers capable of controlling operation of the medical device. Each controller has an active state in which the controller is in communication with, and controls the operation of, the medical device, and a passive state in which the controller is not controlling operation of the medical device. At any given time only one of the plurality of controllers will be in the active state and a remainder of the plurality of controllers will be in the passive state. The active controller may be configured to continually communicate with the remainder of passive controllers, without using the medical device as an intermediary, to update the information stored in the memories of the passive controllers to match the information in the memory of the active controller.

Abstract: A connector assembly including a female element having a bore with an open end. A male element is insertable into the bore of the female element along an axis in a first axial direction and removable from the bore of the female element in a second axial direction. One of the female and male elements defines a circumferential surface extending around the axis and a depression in the circumferential surface, the depression having a catch wall facing in one of the first and second axial directions and a release wall facing in the other one of the first and second axial directions. A second one of the male and female elements has a finger mounted thereon, the finger has a catch end biased in a radial direction transverse to the axis, the catch end of the finger being configured to engage the depression and abut the catch wall.

Abstract: A mechanical circulatory support device includes an inner housing having an inlet end, an outlet end, and a flow path there between. The flow path defines a longitudinal axis. A volute downstream of the outlet end has an outlet port. A rotor mounted within the inner housing upstream of the volute and configured to rotate about the longitudinal axis is included. The volute includes an inner surface having a minimum radius immediately adjacent the rotor and a maximum radius at the outlet port that is larger than the minimum radius.

Abstract: A signal processing circuit for controlling operation of an implanted ventricular assist device comprising an input module for receiving one or more signals of a patient from one or more sensors. A processor for processing the received signals is included, the processor configured to compare a total blood output on a left side of the patient's heart with a total blood output on a right side of the patient's heart; determine at least one from the group consisting of the presence of fluid imbalance between the left and right sides of the patient's heart and the absence of fluid imbalance between the left and right sides of the patient's heart based on the comparison; and when the presence of fluid imbalance is determined, control the implanted ventricular device to restore fluid balance between the left and right sides of the patient's heart.

Abstract: The present disclosure relates to an improved transcutaneous energy transfer (TET) system that generates and wirelessly transmits a sufficient amount of energy to power one or more implanted devices, including a heart pump, while maintaining the system's efficiency, safety, and overall convenience of use. The disclosure further relates one or more methods of operation for the improved system.

Abstract: A tool for coring a hole in a patient's body. A housing includes a first opening and a second opening and has an axis extending therebetween. A shaft is movably positioned along the axis. A blade assembly is attached to one end of the shaft. The blade assembly comprises a cup having an open end and a closed end and a cutting edge formed around the open end. An interface is attached to the housing, which is shaped and dimensioned to communicate with a connector used to connect a medical device to a the patient's body.

Abstract: The present disclosure provides for each of a method of characterizing divergence of a monitored flow rate of blood through an implantable blood pump, and a method of predicting an upcoming adverse cardiac event using operating data of the blood pump, such as the characterized divergence data. Predicting an upcoming adverse cardiac event may be further based on similar operating data from a plurality of other implantable blood pumps.

Abstract: A tunneling device for creating a pathway in subcutaneous tissue of a person's body. The tunneling device includes a member having two ends, where each of the ends defines an insertion surface that facilitates the insertion of the ends into the subcutaneous tissue of the person's body. The tunneling device includes an interchangeable handle connectable to each of the ends. The handle defines a grasping surface and an opening. The opening is configured to receive either of the ends. The grasping surface enables a user to securely hold the handle with one hand to forcibly move the member through the subcutaneous tissue of the person's body to create the pathway in the subcutaneous tissue, and pull a cable of an implant device through the created pathway.