Patent classifications
A61B2560/0204
Determining non-transmission time of a terminal device based on a non-supply of power
An information generation device includes: a receiver configured to receive physiological information of a subject, from a terminal device configured to operate by power of a battery, and continuously acquire and transmit the physiological information; a determination unit configured to determine whether non-transmission time, during which the terminal device is not capable of transmitting the physiological information to the receiver since the power is not supplied to the terminal device, is equal to or longer than predetermined time; and a generator configured to generate first alert information indicating that the non-transmission time is equal to or longer than the predetermined time, when the determination unit determines that the non-transmission time is equal to or longer than the predetermined time.
NON-INVASIVE HYDRATION AND ELECTROLYTE MONITORING
A system for detecting salt ion concentration, comprising a device further comprising a sensor having a carbon printed electrode on a flexible substrate with adhesive on one side (backside) and the circuit electronics to generate pulse signal stimuli and measure salt concentrations to determine hydration level of a person or a living being, wherein the device is a wearable device. The electrode can be made into different shapes changing the area as necessary, since it is a carbon printed electrode and is flexible.
Apparatus and method for intravascular measurements
Intravascular diagnosis apparatus and methods are disclosed. In one aspect of the disclosed technology, a intravascular diagnosis apparatus includes a monitoring guidewire and a display unit. The monitoring guidewire includes a core wire and a sensor disposed in a distal region of the core wire. The display unit includes a processor and a display screen, and is capable of receiving communication from the monitoring guidewire. The display unit is configured to perform computations using the processor based on communications received from the monitoring guidewire and is configured to display information on the display screen based on the computations. The display unit can be configured to be disposed after a predetermined number of uses or after a predetermined duration of use.
Charging station for physiological monitoring device
A charging station for providing power to a physiological monitoring device can include a charging bay and a tray. The charging bay can include a charging port configured to receive power from a power source. The tray can be positioned within and movably mounted relative to the charging bay. The tray can be further configured to secure the physiological monitoring device and move between a first position and a second position. In the first position, the tray can be spaced away from the charging port, and, in the second position, the tray can be positioned proximate the charging port, thereby allowing the physiological monitoring device to electrically connect to the charging port.
Medical device integrated with portable display and functionality
A system is provided for integrating at least one portable computing device with a resuscitative medical device such as a defibrillator. The system may include a carrying case coupled to the resuscitative medical device. The carrying case may include a storage space for the at least one portable computing device and a wireless charging system for charging the at least one portable computing device. The system may be configured to enable secure data transfer between each of the devices, including data communication and data storage. A processor of the resuscitative medical device may be configured to activate the wireless charging system and charge the at least one portable computing device under certain circumstances. The processor may further be configured to prioritize or optimize charging and data transfer between the resuscitative medical device and each of multiple portable computing devices.
MONITOR DEVICE OF A MEDICAL SYSTEM HAVING A CONNECTOR FOR COUPLING TO BOTH A BASE PLATE AND AN ACCESSORY DEVICE
A monitor device for an ostomy system is disclosed. The monitor device comprises a first interface comprising a primary terminal and a secondary terminal. The primary terminal is configured to form electrical connection with a primary electrode of the base plate when the monitor device is coupled to the base plate, and the primary terminal being configured to form electrical connection with a primary charge terminal of the accessory device when the monitor device is coupled to the accessory device. The secondary terminal is configured to form electrical connection with a secondary electrode of the base plate when the monitor device is coupled to the base plate, and the secondary terminal being configured to form electrical connection with a secondary charge terminal of the accessory device when the monitor device is coupled to the accessory device.
Method and apparatus for the capture of intra-cellular activity
An intracellular monitoring device (IMD) that fits completely inside a living cell, and causes no significant impairment, to a cell's normal biological processes. The IMD monitors a cell for its level of a biological substance (e.g., calcium ion concentration) of interest. If the biological substance reaches or exceeds a threshold, the IMD transmits an electromagnetic signal, received by an antenna outside the cell. Each IMD has its electromagnetic signal encoded with a unique frequency. Detection of the frequency components, in the signals received by an antenna, permits identification of the source IMD's. A high calcium ion concentration is indicative of a strongly-activated cerebral cortex neuron. Brain tissue is relatively transparent to near infrared, making it a good frequency band, for the electromagnetic signals from neuron-monitoring IMD's. The near infrared of each IMD can be produced by quantum dots, powered by bioelectric catalysis triggered by high calcium ion concentration.
Power management for an implantable device
Techniques for facilitating improved power management for an implantable device are provided. In one example, an implantable device includes a telemetry circuit and a power management circuit. The telemetry circuit is configured to facilitate a telemetry session between the implantable device and an external device. The power management circuit is configured to connect a power supply to the telemetry circuit via a first current-limiting device based on a determination that the telemetry circuit satisfies a defined criterion. The power management circuit is also configured to connect the telemetry circuit to a second current-limiting device based on a determination that the telemetry circuit is connected to the first current-limiting device for a defined period of time.
Methods and Systems for Tremor Reduction
A tremor-reduction system is provided that delivers electric current to a body region of a subject that is associated with a tremor. A computing device stores received data associated with a tremulous movement of the body region and determines measurements associated with the stored data. If a magnitude of the most recent tremulous movement is the same as or greater than magnitudes associated with prior tremulous movements, characteristics of a subsequent electric current to be applied to the body region may be adjusted.
RESPIRATORY MONITORING DEVICE
There is provided a respiratory monitoring device (100) comprising one or more respiratory-related sensors (110) and a first circuit board comprising a controller. The one or more respiratory-related sensors are separated from and in communication the first circuit board. There is also provided a respiratory monitoring device comprising a controller, one or more respiratory-related sensor and an input means (114). The input means is arranged to trigger the controller to suspend sensing by at least one of the one or more respiratory-related sensors for one or more predetermined time periods. There is also provided a respiratory monitoring device having a housing comprising a front surface (102) at which one or more respiratory-related sensors are arranged, and a back surface (120), wherein the front surface is arranged to indicate an intended orientation to a user of the respiratory monitoring device.