TC1 LLC

Sensors for catheter pumps are disclosed herein. The catheter pump can include a catheter assembly comprising a catheter and a cannula coupled to a distal portion of the catheter. The cannula can have a proximal port for permitting the flow of blood therethrough. The catheter assembly can include a sensor to be disposed near the proximal port. A processing unit can be programmed to process a signal detected by the sensor. The processing unit can comprise a computer-readable set of rules to evaluate the signal to determine a position of the cannula relative to an aortic valve of a patient.

An enclosure for an implantable device is provided. The enclosure includes a cup defining a cavity, the cup including a non-metallic body, and a weld ring coupled to the non-metallic body, and a lid, wherein the lid is weldable to the weld ring to couple the cup to the lid and hermetically seal the enclosure.

A catheter pump assembly is provided that includes an elongate body, an elongate flexible shaft disposed in the elongate body, and an impeller coupled with the distal end of the elongate flexible shaft. The drive system includes a drive component, a motor and a tension member. The tension member is coupled with the motor and the drive component and to cause the drive component to rotate, and thereby to cause the impeller to rotate.

Systems and related methods for supplying power to a medical device. A medical system includes a medical service and a base module. The medical device is configured to be worn by a user or implanted in the user. The base module is configured to control operation of the medical device and supply electrical power to the medical device. The base module includes a base module input connector that includes two power connectors, two ground connectors, and a data connector arranged in a symmetrical arrangement that accommodates two opposite connection orientations of a mating input connector with the base module input connector.

A catheter pump assembly is provided. The catheter pump assembly includes a proximal portion, a distal portion, a catheter body having a lumen extending along a longitudinal axis between the proximal and distal portions, an impeller disposed at the distal portion, and a stator disposed at a downstream location of the impeller to straighten flow downstream from the impeller. The stator is collapsible from a deployed configuration to a collapsed configuration.

Blood circulation assist systems with patient connectable cable assemblies. A blood circulation assist system includes a blood pump, an external controller, a percutaneous cable assembly, and an external cable assembly. The external controller is configured to output a connection indication. The percutaneous cable assembly includes a proximal connector. The external cable assembly includes a distal connector. The distal connector and the proximal connector are configured for connection and disconnection by the patient. The external controller is configured to detect whether the distal connector and the proximal connector are connected. The connection indication is indicative of whether the distal connector and the proximal connector are connected.

Systems and methods for connections in a medical device system are provided. A connector system includes a connector receptacle including first electrical contacts, a connector insert including second electrical contacts and at least one pin, and a locking member rotatably coupled to the connector receptacle, the locking member including a housing and a guide member, the guide member including an annular body that defines at least one groove including a first locking detent and a second locking detent, the at least one pin operable to traverse the at least one groove, engage the first locking detent in a first locked configuration, and engage the second locking detent in a second locked configuration when the connector insert is inserted into the connector receptacle.

A system for collecting real-time on-demand measurements. The system includes an implantable sensor that has a power source, a sensing circuit, a communications circuit, a memory, and one or more processors. The sensing circuit senses a physiologic parameter of interest (PPOI) and generates signals indicative of the PPOI. The communications circuit communicates with at least one of an implantable medical device (IMD) or an external device (ED). The one or more processors execute program instructions stored in the memory to collect real-time on-demand measurements by activating the sensing circuit to generate the signals indicative of the PPOI, converting the signals to physiologic data indicative of the PPOI, storing the physiologic data in the memory, and directing the communications circuit to transmit the physiologic data to the at least one of the IMD or the ED.

Mutual authentication ana encryption key generation for secure wireless communication between an implantable medical device and an external device employs asymmetric cryptography. A method of conducting secure wireless communication between an implantable medical device and an external device includes conducting a mutual authentication procedure that employs asymmetric cryptography via wireless communication between the implantable medical device and the external device. A shared encryption key is generated by the external device. The shared encryption key is generated by the implantable medical device. Wireless communication is conducted between the implantable medical device and the external device via wireless transmissions encrypted via the shared encryption key.

Systems for automated patient management employ remote patient monitoring to trigger transmission of clinician defined interventional treatment instructions in response to satisfaction of clinician defined triggering criteria. A system for automated patient management execute a clinician portal module configured to receive pulmonary artery pressure data generated via a pulmonary artery pressure sensor, receive input defining a pulmonary artery pressure based interventional treatment triggering criteria, receive input defining interventional treatment instructions, process the pulmonary artery pressure data to determine whether the pulmonary artery pressure based interventional treatment triggering criteria is satisfied by the pulmonary artery pressure data, and in response to determining that the pulmonary artery pressure based interventional treatment triggering criteria is satisfied by the pulmonary artery pressure data, transmit the interventional treatment instructions to a patient mobile application.