A system for minimizing misalignment notifications for a TETS having an implantable blood pump, an external controller having a power source and a processing circuitry, a transmission coil in communication with the external controller, a receiving coil configured for transcutaneous inductive communication with the transmission coil, and an implantable controller in communication with the receiving coil and the implantable blood pump. The implantable controller having a power source configured to receive power from the receiving coil. The processing circuitry may be configured to: operate in a first mode where an alert is generated when a power efficiency transfer between the transmission coil and the receiving coil is below a first predetermined threshold; and operate in a second mode where the alert is only generated when the power remaining in the power source for the implantable controller is below a first predetermined power source threshold.

A system for minimizing misalignment notifications for a TETS having an implantable blood pump, an external controller having a power source and a processing circuitry, a transmission coil in communication with the external controller, a receiving coil configured for transcutaneous inductive communication with the transmission coil, and an implantable controller in communication with the receiving coil and the implantable blood pump. The implantable controller having a power source configured to receive power from the receiving coil. The processing circuitry may be configured to: operate in a first mode where an alert is generated when a power efficiency transfer between the transmission coil and the receiving coil is below a first predetermined threshold; and operate in a second mode where the alert is only generated when the power remaining in the power source for the implantable controller is below a first predetermined power source threshold.

The present invention relates to a filtering device for removing particles from a bodily fluid of a patient, the filtering device being implantable in the patient's body. The device has a tube forming a main fluid passageway for bodily fluid, through which the bodily fluid of the patient passes when the tube is implanted in the patient, a filter connected to the tube and a filter cleaning device for cleaning the filter by moving particles collected by the filter out of the fluid passageway, wherein the filter cleaning device is adapted to replace the first filter in the fluid passageway with a second filter, thereby moving the particles collected by the first filter out of the fluid passageway.

The present invention relates to a filtering device for removing particles from a bodily fluid of a patient, the filtering device being implantable in the patient's body. The device has a tube forming a main fluid passageway for bodily fluid, through which the bodily fluid of the patient passes when the tube is implanted in the patient, a filter connected to the tube and a filter cleaning device for cleaning the filter by moving particles collected by the filter out of the fluid passageway, wherein the filter cleaning device is adapted to replace the first filter in the fluid passageway with a second filter, thereby moving the particles collected by the first filter out of the fluid passageway.

A connector assembly for use in a medical device system is provided. The connector assembly includes a female connector including a jack and at least one female electrical contact disposed in the jack, where the at least one female electrical contact includes an outer ring and leaf springs extending both radially inward from the outer ring and longitudinally along the jack. The connector assembly also includes a male connector including a plug adapted to be inserted into the jack of the female connector, and at least one male electrical contact disposed on the plug, where the at least one male electrical contact is configured to electrically couple to a corresponding female electrical contact of the at least one female electrical contact by contacting the plurality of leaf springs of the corresponding female electrical contact when the plug of the male connector is inserted into the jack of the female connector.

A connector assembly for use in a medical device system is provided. The connector assembly includes a female connector including a jack and at least one female electrical contact disposed in the jack, where the at least one female electrical contact includes an outer ring and leaf springs extending both radially inward from the outer ring and longitudinally along the jack. The connector assembly also includes a male connector including a plug adapted to be inserted into the jack of the female connector, and at least one male electrical contact disposed on the plug, where the at least one male electrical contact is configured to electrically couple to a corresponding female electrical contact of the at least one female electrical contact by contacting the plurality of leaf springs of the corresponding female electrical contact when the plug of the male connector is inserted into the jack of the female connector.

An external power transmitter of an implanted medical device system such as a left ventricular assist device (LVAD) system and a method therefore are provided. According to one aspect, a method includes transitioning from applying a first external coil current limit to applying a second external coil current limit to limit current of an external coil coupled to the external power transmitter, the transitioning being based on at least one of an intent to enter a free mode of operation of the implanted medical device system, an existence of an alarm condition, and an existence of transcutaneous energy transfer system (TETS) power transfer.

An external power transmitter of an implanted medical device system such as a left ventricular assist device (LVAD) system and a method therefore are provided. According to one aspect, a method includes transitioning from applying a first external coil current limit to applying a second external coil current limit to limit current of an external coil coupled to the external power transmitter, the transitioning being based on at least one of an intent to enter a free mode of operation of the implanted medical device system, an existence of an alarm condition, and an existence of transcutaneous energy transfer system (TETS) power transfer.

Systems and related methods for supplying power to a medical device employ serially-connectable portable batteries. A method of supplying electrical power to a medical device includes discharging a first external battery to output electrical power to a second external battery. Distribution of the electrical power received by the second external battery is controlled to simultaneously charge the second external battery and output electrical power from the second external battery to supply electrical power to the medical device.

A bearingless and sealless rotary blood pump is disclosed which provides multidirectional flow intended to provide low-pressure, high-volume right-sided partial assist circulatory support in a univentricular Fontan circulation on a permanent basis. The pump includes a housing and an impeller suspended in the center of the housing. The housing incorporates flow optimization features between inlet and outlet ends, as well as with the impeller surface. Large fluid gaps maintained between impeller and housing eliminate any potential for blood flow obstruction. The impeller contains some motor components. It includes a central stator and surrounding rotor. The motor includes a brushless DC outrunner electrical motor design. An electromagnetic stator core is surrounded by a circumferential passive magnetic ring. The rotor is further levitated about the stator spindle by a plurality of axially and radially located passive magnetic and hydrodynamic journal bearings on both ends of the spindle. The rotor is bearingless and sealless. During impeller rotation, blood entering the space between the rotor and stator is induced to flow by centrifugal pumping action and the fluid film separates the stator hydrodynamic bearings from the rotor so that there is no direct mechanical contact between the rotor and stator.