A lighting system for establishing a database of multispectral circadian rhythm lighting scenario and psychological stress indicators is configured in space, which is characterized by downloading the multispectral circadian rhythm lighting scenario database from the cloud; the multispectral lighting parameters and circadian rhythm parameters are selected from the multispectral circadian rhythm lighting scenario database to start the light-emitting device for lighting; the ambient light sensor measures and judges whether the circadian rhythm parameters reach the set value; when each circadian rhythm parameter in the circadian rhythm lighting scenario database has reached the set value, the light-emitting device is started for lighting; after the blood or saliva of the light control subjects were tested, the psychological stress index values of the illuminators were obtained; the portable communication device transmits the circadian rhythm parameters and psychological stress index values to the cloud; among them, the circadian rhythm parameters include: circadian rhythm lighting parameters and circadian rhythm scenario parameters.

A computer-based system for receiving, analyzing, processing, managing and sending personal health information, and other information in conjunction with use of one or more personal nebulizer or vaporizing devices and personal breath analysis devices. System devices include a personal nebulizer or vaporizing unit with a mouthpiece, which may be detachable and replaceable. The mouthpiece includes an orifice through which vapor is emitted. The substance to be vaporized is contained in an ampoule inserted into the device, where the substance enters an atomization chamber where vaporization is achieved through piezoelectric transducers or atomizers providing sonic or ultrasonic vibration. The substance includes a variety of therapeutic, homeopathic, or naturopathic formulations, remedies, or serums.

A method of reducing the risk of ventilator-associated pneumonia by decontaminating the oropharynx using a safe, antimicrobial light-emitting device.

A fluid injector system includes a powered fluid injector, a connection port configured to receive a single-use disposable set having tubing connected to a fluid inlet port at a first end and connected to a waste outlet port at a second end, and a detector associated with the connection port and configured to generate a signal in response to a sonic, infrasonic, or ultrasonic wave emitted from the single-use disposable set during a priming operation of the single-use disposable set. In some examples, the detector is configured to generate a signal if the frequency of the wave emitted from the single-use disposable set is outside a predetermined range of frequencies corresponding to a predetermined range of frequencies of air expelled from the tubing. A method for detecting the multiple uses of a single-use disposable set connected to a fluid injector system is also provided.

Injection monitoring circuitry is provided for coupling to part of an injection device having a syringe and a plunger rod. The injection monitoring circuitry has an input to receive force measurement data from a force sensor, the force measurement data includes a plurality of timestamped force measurements of force applied by a user to the injection device when an injection is administered to an injection site. Processing circuitry is provided to determine from the force measurement data when an end of injection has been reached, the end of injection corresponding to the plunger rod having reached an end position in a distal portion of the barrel of the syringe during administration of the injection by the user. Machine readable instructions and an injection monitoring method are also provided.

Disclosed herein are facially fitting devices, such as nasal cannulas and oxygen masks, including illuminating placement marker(s), which facilitate correct placement of the facially fitting devices on a face of a subject in dark conditions. The placement marker is powered by a thermo-electric generator, which generates electrical power via thermal coupling thereof to skin on the face of a subject when the facially fitting device is fitted, or partially fitted, on the face of the subject.

The disclosure relates to a detector arrangement for detecting a position of an object with regard to a first direction, wherein the object includes a front edge and a rear edge separated from each other in the first direction and wherein the object is movable relative to the detector arrangement in the first direction. The detector arrangement includes a first detector configured to detect electromagnetic radiation, the first detector including a first detection area sensitive to the electromagnetic radiation, wherein the detection area is confined by a first detection front edge and by a first detection rear edge, wherein the first detection front edge is separated from the first detection rear edge in the first direction. At least one of the first detection front edge and the first detection rear edge extends non-parallel to at least one of the front edge and the rear edge of the object.

A data collection device comprises an attachment assembly for attaching the data collection device to a dose setting dial of a medicament administration device and a sensor configured to detected an identifier provided on a surface of an internal component of the medicament administration device, the sensor comprising an ultrasound sensor configured to detect a geometric identifier formed on the surface of the internal component of the medicament administration device. A system comprises the data collection device and the medicament administration device.

A filling aid device for filling a reservoir. The device includes a cover portion comprising a septum window; a slider beam comprising a septum cover; and a first filling aid tab attached to the slider beam, the first filling aid tab in slidable relation to the cover from a first position to a second position, wherein when the filling aid device is in an unlocked position, the septum cover is located below the septum window, wherein when the first filling aid tab is moved from the first position to the second position, the septum cover is moved from below the septum window, and the filling aid device is in the locked position.

In some embodiments, a medical system includes a dialysis machine having at least one outer surface to be disinfected at a given location, at least one disinfection sensor connected to the dialysis machine at the given location, the disinfection sensor including two or more electrode in fluid contact with the outside surface of the dialysis machine, and a conductivity sensor component in electrical contact with the two or more electrodes, the conductivity sensor component configured to send an electrical signal indicating a conductivity of a liquid on an outside surface of the dialysis machine and in contact with the two or more electrodes, a processor configured to receive the electrical signal and thereby determine a disinfection status of the given location, and a user interface configured to indicate the disinfection status of the given location.