The present disclosure presents systems, apparatuses, and methods of evaluating air quality sensor data. In this regard, a method comprises receiving air quality sensor data from a plurality of portable smart air quality measurement system (SAQMS) communication devices from a plurality of citizens in a geographic location; receiving air quality sensor data from an air quality measurement and calibration (AQMC) station in the geographic location; determining a level of resolution for one or more sensors of a portable SAQMS communication device at a central evaluation and measurement service; correcting air quality data received from the portable SAQMS communication device to compensate for the determined level of resolution at the central evaluation and measurement service; and generating a map of air quality data based on at least the corrected air quality data of the portable SAQMS communication device and a plurality of other portable SAQMS communication devices.

A diagnostic transceiver assembly includes a diagnostic unit that may be implanted into a human body. The diagnostic unit monitors physiological functions of the human body to include heart rate and blood serum levels. The diagnostic unit generates a diagnostic sequence when the diagnostic unit detects blood serum levels outside of a trigger ratio. A dispensing unit may be implanted into the human body. The dispensing unit is in fluid communication with the human circulatory system. The dispensing unit contains insulin. The dispensing unit releases a measured amount of the insulin into the human circulatory system in response to the diagnostic sequence.

An electronic cigarette includes a shell and a mouthpiece. The external wall of the shell has an air inlet. An atomizer and a liquid-supply are in contact with each other. The air inlet, atomizer, and an aerosol passage are interconnected.

Provided is a wearable, self-contained drug infusion or medical device capable of communicating with a host controller or other external devices via a personal area network (PAN). The medical device utilizes a PAN transceiver for communication with other devices in contact with a user's body, such as a physiological sensor or host controller, by propagating a current across the user's body via capacitive coupling. The wearable nature of the medical device and the low power requirements of the PAN communication system enable the medical device to utilize alternative energy harvesting techniques for powering the device. The medical device preferably utilizes thermal, kinetic and other energy harvesting techniques for capturing energy from the user and the environment during normal use of the medical device. A system power distribution unit is provided for managing the harvested energy and selectively supplying power to the medical device during system operation.

Systems and techniques for enhanced sleep tracking, monitoring, and conditioning are discussed herein. A device may be couplable to, or integrally formed with, a piece of furniture (a “nearable”) receives sensor data from one or more sensors accessible to the device and, based on a determined stage of sleep, may actuate one or more devices for conditioning sleep. In some examples, the nearable may be configured to receive a smartphone such that one or more processors and sensors of the smartphone may be used to perform at least some of the processes. When configured to receive a smartphone, the nearable's cavity may retain the smartphone via a spring mechanism to create an additional button for user interaction, as well as be shaped to minimize an amount of electromagnetic radiation (including light emitted from a screen) of the smartphone, while optimizing sounds output from the smartphone.

The present disclosure discloses a device for automatically collecting snot, which comprises a suction nozzle, a collecting cup, a cup holder and a shell component which are detachably connected in sequence, wherein the shell component is a hollow cavity. The present disclosure generates negative pressure suction through the air pump, and then the suction air enters the inner collecting cup through the air suction pipe, the cup holder air inlet, the air inlet channel and the micropore in sequence. Finally, the suction sucks the snot in the nose of a user into the inner collecting cup through the suction nozzle, effectively solving the problem of snot reflux.

An infusion pump which may include a control unit and a pump engine may be used to facilitate administration of medicinal fluids to a patient. A control unit may include a motor, a controller, a housing, and a motor coupling, where the motor coupling includes two protruding motor coupling tabs extending in a direction parallel to an output shaft of the motor. A pump engine may include a housing, a rotor disposed in the housing, and a pump coupling, where the pump coupling includes at least two protruding pump coupling tabs extending in a direction parallel to an input shaft of the rotor. The controller may be configured to change an operational mode of the infusion pump, where when the infusion pump is in a positioning mode, the controller activates the motor to move the output shaft to a predetermined angular position.

A night light may include a night light housing, a light source associated with the housing, a speaker associated with the housing, a controller configured to control operations of the night light, a stand adapted to receive the housing a charge a battery associated with the housing to power the operations of the night light, and a sensor associated with the housing configured to detect when the housing is positioned on the stand or when the housing is not positioned on the stand. The controller may be configured to reduce sound volume output from the speaker, or disable a wireless communication port associated with the housing when the housing is not detected to be positioned on the stand.

A negative pressure wound therapy system includes a wound dressing, at least one pump fluidly coupled to the fluid interface, a pressure sensor fluidly coupled to the wound dressing, a control housing, and an electrical coupler. The wound dressing includes a sealing layer, an absorbent layer adjacent to the sealing layer, and a fluid interface attached to at least one of the sealing layer or the absorbent layer. The at least one pump is configured to apply negative pressure to the fluid interface to draw fluid from the wound dressing via the fluid interface. The pressure sensor is configured to detect a fluid pressure of the wound dressing. The control housing is remote from the wound dressing. The electrical coupler is configured to removably connect the control housing to the at least one pump.

A programmable memory device for incorporation within a medium to distribute a force or shock, F, within the medium. It includes a programmable combination of micro-levers that cooperate in order to selectively disperse, absorb, redirect, reorient, or displace, at least part of the force, F, in a customizable fashion. At least one of the micro-levers includes a platform that is supported on a top portion of a support, in order to enable a lever action or momentum of the platform within the medium. As the force, F, is applied on the micro-lever, a reactive force, R, is generated and causes any a movement of the platform relative to the support or a movement of the support relative to the platform, effectively dispersing, absorbing, redirecting, reorienting, or displacing the force, F, within the medium.