A monitoring device having a non-contact physiological parameter monitoring function is disclosed. The monitoring device includes a radio frequency transmission assembly, a radio frequency receiving assembly, a first signal processing circuit and a processor. The radio frequency transmission assembly is configured to generate electromagnetic waves of a specific frequency and transmit the same towards a specific part of a human body. The radio frequency receiving assembly is configured to receive a reflected wave beam reflected back from the specific part of the human body. The first signal processing circuit is configured to convert the reflected wave beam into a first-type physiological parameter signal. The processor is configured to analyze the first-type physiological parameter signal to obtain a first-type physiological parameter value, and to output the first-type physiological parameter value. The psychological parameter values of a patient are acquired in a non-contact manner, thereby improving the convenience and safety of operation.

The present embodiments relate generally to apparatuses, systems, and methods for deploying a medical device to skin of a host. The apparatuses, systems, and methods may be directed to removing a liner for a medical device so that the medical device may couple to the skin of the host. The medical device may comprise an on-skin wearable medical device.

A system for displaying information indicative of driving conditions, to a driver, using a smart ring are disclosed. An exemplary system includes a smart ring with a ring band having a plurality of surfaces including an inner surface, an outer surface, a first side surface, and a second side surface. The system further includes a processor, configured to obtain data from a communication module within the ring band, or from one or more sensors disposed within the ring band. The obtained data are representative of information indicative of one or more driving conditions to be displayed to the driver. The smart ring also includes an electronic ink (e-ink) display disposed on at least one of the plurality of surfaces, and configured to present information indicative of the one or more driving conditions.

A system and method for monitoring body chemistry of a user, the system comprising: a housing supporting: a microsensor comprising a first and second working electrode, a reference electrode, and a counter electrode, and configured to access interstitial fluid of the user, and an electronics subsystem comprising a signal conditioning module that receives a signal stream, from the microsensor, wherein the electronics subsystem is configured to detect an impedance signal derived from two of the first working electrode, the second working electrode, the reference electrode, and the counter electrode; and a processing subsystem comprising: a first module configured to generate an analysis indicative of an analyte parameter of the user and derived from the signal stream and the impedance signal, and a second module configured to transmit information derived from the analysis to the user, thereby facilitating monitoring of body chemistry of the user.

Technologies for providing a cognitive capacity test for autonomous driving include a compute device. The compute device includes circuitry that is configured to display content to a user, prompt a message to the user to turn user’s attention to another activity that needs situational awareness, receive a user response, and analyze the user response to determine an accuracy of the user response and a response time, wherein the accuracy and response time are indicative of a cognitive capacity of the user to assume control of an autonomous vehicle when the autonomous vehicle encounters a situation that the vehicle is unable to navigate.

An application running in a mobile device displays an ultrasound image obtained by a connected ultrasound scanner. A button is displayed on the device, which, when activated, automatically connects the device to a remote reviewer in a virtual videoconferencing room, without the operator of the scanner needing to input user credentials. Upon activating the button, or otherwise triggering the request for a review, pre-stored login credentials are automatically retrieved and used for connecting the operator to the room. The remote reviewer may be connected to the room upon accepting the request for review, without having to input user credentials, which are pre-stored and automatically retrieved.

A pulmonary neuromuscular metrics device that allows the measurement of pulmonary neuromuscular metrics, that is, breathing power, force, and work (that is, energy expended), in patients with neuromuscular conditions. The device may be used in the medical office or remotely at a patient's house, thereby allowing the patient to be followed medically without the need for more frequent and repeated office visits.

A health monitoring system comprises at least one sensor configured to measure at least one parameter relating to a condition of a subject; and a health monitoring module in communication with the at least one sensor and configured to receive from the at least one sensor a measurement of the at least one parameter; based on the measurement, generate a message; and send the message to a health operator related to the subject. Moreover, in some embodiments, the health monitoring module is further configured to determine a confidence factor for the measurement. Further, in some embodiments the health monitoring module is also configured to receive from the at least one sensor a plurality of measurements of the at least one parameter; derive a trend for the plurality of measurements; and based on the trend, determine a health state for the subject.

A system for predicting an adverse reaction of a patient, based on a real-time bio-signal of the patient, according to an embodiment of the disclosure, may include: a bio-signal measurement device configured to measure a bio-signal of the patient at a first time interval and transmit a measured result to a patient terminal at the first time interval; the patient terminal configured to collect the bio-signal measured at the first time interval from the bio-signal measurement device and transmit the collected bio-signal to a server at a second time interval; the server configured to receive the bio-signal from the patient terminal at the second time interval, based on the received bio-signal, identify whether a predetermined action is necessary for the patient at the second time interval, and when the predetermined action is necessary, transmit a message to a medical team terminal; and the medical team terminal configured to receive the message from the server when the predetermined action is necessary.

A base plate and/or a sensor assembly part for an ostomy appliance is disclosed, the base plate and/or the sensor assembly part comprising a first adhesive layer with a proximal side configured for attachment of the base plate and/or the sensor assembly part to the skin surface of a user, the first adhesive layer having a stomal opening with a center point; and a plurality of electrodes including a ground electrode, a first electrode, and a second electrode, the ground electrode comprising a ground connection part, the first electrode comprising a first connection part, and the second electrode comprising a second connection part; wherein the ground electrode forms a ground for the first electrode and the second electrode.