Abstract: In general, the invention is directed to a system with a fail-safe mode for remote programming of medical devices, such as implantable medical devices (IMDs). During a remote programming session, an adverse event, such as a programming session failure, may prevent proper completion of a programming or result in improper programming due to data corruption or other factors. If a programming session is not completed correctly, the IMD is susceptible to improper operation, possibly exposing a patient to delivery of unnecessary or inappropriate therapies. A fail-safe mode reduces the likelihood of improper operation following a programming session failure. The fail-safe mode defines one or more fail-safe operations designed to preserve proper operation of the IMD. In some embodiments, the fail-safe operations include notifying a person concerning the failure of the programming session, modifying programming parameters within the implantable medical device, and delivering a therapy to a patient.

Abstract: A combined ionic air filter and humidifier apparatus filters air using ionic air filtering, humidifies at least a portion of the filtered ionized air, and directs the humidified filtered ionized air back into the environment. The apparatus generally includes an ionic air filter for ionizing and filtering air to produce filtered ionized air and a humidifier for humidifying the filtered ionized air to produce humidified filtered ionized air. A humidifier manifold fluidly couples the humidifier with the ionic air filter in a manner that does not allow the humidifier to interfere with operation of the ionic air filter. One or more fans draw the air into the ionic air filter and direct at least a portion of the filtered ionized air into the humidifier manifold such that the humidified filtered ionized air is discharged from the humidifier manifold.

Abstract: A combined ionic air filter and humidifier apparatus filters air using ionic air filtering, humidifies at least a portion of the filtered ionized air, and directs the humidified filtered ionized air back into the environment. The apparatus generally includes an ionic air filter for ionizing and filtering air to produce filtered ionized air and a humidifier for humidifying the filtered ionized air to produce humidified filtered ionized air. A humidifier manifold fluidly couples the humidifier with the ionic air filter in a manner that does not allow the humidifier to interfere with operation of the ionic air filter. One or more fans draw the air into the ionic air filter and direct at least a portion of the filtered ionized air into the humidifier manifold such that the humidified filtered ionized air is discharged from the humidifier manifold.

Abstract: System and method for interfacing with a medical device having a host device and a communication module. The host device has a user interface configured to input and display information relating to the interfacing with the medical device. The communication module is locally coupled to the host device and configured to communicate wirelessly with the medical device. The system, implemented by the host device and the communication module, is configured to communicate with the medical device with functions. The system, implemented by at least one of the host device and the communication module, has a security condition. At least one of the functions is disabled, at least in part, from operating on the system based upon the security condition.

Abstract: An aerator for aerating a liquid within a container having a main body portion and an opening. The aerator includes a pump assembly configured to provide an air flow, a cannulated shaft, and a manifold assembly configured to be fluidly coupled to the pump assembly by way of the cannulated shaft. The manifold assembly is configured to distribute the air flow to a plurality of radially arranged manifold nozzles, wherein the radially arranged manifold nozzles are configured to generate a plurality of air bubbles having a radial velocity configured to direct the plurality of air bubbles radially outward from the manifold assembly such that the plurality of air bubbles travel vertically upwards generally towards the opening of the container without generally contacting the main body portion of the container or the cannulated shaft. For example, the manifold assembly may be configured to generate the plurality of air bubbles having a radial velocity of 2.0 feet/second to 3.0 feet/second.

Abstract: A system with a medical device, an interface device and a communication controller. A medical device has a medical device communication module. The interface device has an interface device communication module and a user interface operatively coupled to the interface device communication module and configured to communicate with a user of the system. The communication controller has a communication controller module configured to communicate with the medical device communication module and with the interface device communication module and an information server operatively coupled to the communication controller module and configured to drive the user interface of the interface device. The system is configured so that a user of the system may communicate with the medical device using the user interface of the interface device with the user interface of the interface being driven by the information server of the communication module.

Abstract: System and method for providing medical information concerning a patient having first patient physiological data and second patient physiological data. The system has a medical device and a handheld device. The medical device is configured to be implanted in the patient and has a sensor configured to obtain the first patient physiological data and a communication module. The handheld device has a communication module, a processor and a user interface. The device communication module is configured to communicate with the medical device communication module, the device communication module being configured to transfer the first patient physiological data to the handheld device via the communication module. The processor is configured to combine the first patient physiological data and the second patient physiological data and generate feedback having a recommended course of action based, at least in part, on the first patient physiological data and the second patient physiological data.

Abstract: System and method for interfacing with a medical device. The system has a host device and a communication module. The host device has a user interface configured to input and display information relating to the interfacing with the medical device. The communication module is locally coupled to the host device and configured to communicate wirelessly with the medical device. The system, implemented by the host device and the communication module, is configured to communicate with the medical device with functions. The system, implemented by at least one of the host device and the communication module, has validation layers configured for use by users, each of the users having access to at least one of the validation layers based on a validation condition, each individual one of the functions being operational through the user interface only with one of the validation layers.

Abstract: System and method for interfacing with a medical device having a host device and a communication module. The host device has a user interface configured to input and display information relating to the interfacing with the medical device. The communication module is locally coupled to the host device and configured to communicate wirelessly with the medical device. The system, implemented by the host device and the communication module, is configured to communicate with the medical device with functions. The system, implemented by at least one of the host device and the communication module, has a security condition. At least one of the functions is disabled, at least in part, from operating on the system based upon the security condition.

Abstract: In general, the invention is directed to a system with a fail-safe mode for remote programming of medical devices, such as implantable medical devices (IMDs). During a remote programming session, an adverse event, such as a programming session failure, may prevent proper completion of a programming or result in improper programming due to data corruption or other factors. If a programming session is not completed correctly, the IMD is susceptible to improper operation, possibly exposing a patient to delivery of unnecessary or inappropriate therapies. A fail-safe mode reduces the likelihood of improper operation following a programming session failure. The fail-safe mode defines one or more fail-safe operations designed to preserve proper operation of the IMD. In some embodiments, the fail-safe operations include notifying a person concerning the failure of the programming session, modifying programming parameters within the implantable medical device, and delivering a therapy to a patient.