A multi-sensory media experience delivery platform includes a vibroacoustic therapy bed that delivers a multi-sensory media experience locally stored, streaming, on-demand, or real-time signals. The vibroacoustic therapy bed drives a plurality of sensory output devices based on a set of sensory output channels to produce sounds, vibrations, light patterns, or other sensory outputs. The channels may be derived from dedicated signals created for a specific sensory output device or may be derived from an audio file or other general set of waveforms. The multi-sensory media experience may be customized to a user based on user profile data, metadata associated with the multi-sensory media experience, or biometric data. Furthermore, users can create customized multi-sensory media experiences from libraries of sounds or other media.

A multi-sensory media experience delivery platform includes a vibroacoustic therapy bed that delivers a multi-sensory media experience locally stored, streaming, on-demand, or real-time signals. The vibroacoustic therapy bed drives a plurality of sensory output devices based on a set of sensory output channels to produce sounds, vibrations, light patterns, or other sensory outputs. The channels may be derived from dedicated signals created for a specific sensory output device or may be derived from an audio file or other general set of waveforms. The multi-sensory media experience may be customized to a user based on user profile data, metadata associated with the multi-sensory media experience, or biometric data. Furthermore, users can create customized multi-sensory media experiences from libraries of sounds or other media.

A multi-sensory media experience delivery platform includes a vibroacoustic therapy bed that delivers a multi-sensory media experience locally stored, streaming, on-demand, or real-time signals. The vibroacoustic therapy bed drives a plurality of sensory output devices based on a set of sensory output channels to produce sounds, vibrations, light patterns, or other sensory outputs. The channels may be derived from dedicated signals created for a specific sensory output device or may be derived from an audio file or other general set of waveforms. The multi-sensory media experience may be customized to a user based on user profile data, metadata associated with the multi-sensory media experience, or biometric data. Furthermore, users can create customized multi-sensory media experiences from libraries of sounds or other media.

A bed includes components to control temperature of a sleep surface, for example based on time and historical usage patterns by a user. In some embodiments the temperature of the sleep surface is controlled based on information indicating a sleep state of the user. In some embodiments the temperature is dynamically adjusted so to achieve particular sleep states and/or sleep patterns for the user. In some embodiments the temperature and timing of temperature adjustments is iteratively adjusted over multiple sleep sessions so to achieve improvements in sleep states and/or sleep quality for the user.

A disposable flushing and suction drainage tube and a-using method thereof comprises a flushing tube, a suction tube, and a mounting base. The flushing tube and the suction tube are respectively mounted at one end of the mounting base, and an air connector and a water connector are mounted at the other end; the mounting base comprises a tube body base and a control base, the flushing tube and the suction tube are mounted at one end of the tube body base, and the other end is detachably connected to the control base. The disposable flushing and suction drainage tube controls suction for the suction tube by a negative pressure adjusting opening on the mounting base; opening, closing, and water flow of the flushing tube is controlled by a water control switch on the mounting base, and switching between flushing and drainage and the flow of drainage can be controlled.

A phototherapy device (100) and a phototherapy instrument (500), comprising a near infrared irradiation module (110) used for emitting near infrared light to the head, and a control component (120) used for controlling the operation of the near infrared irradiation module (110) and coupled to the near infrared irradiation module (110). A method for using near infrared light for therapy, which comprises applying a first, optional second, optional third or more near infrared lights to the head of a patient. The device and method are used for treating Alzheimer's disease, improving brain mitochondrial function and ATP levels, promoting amyloid beta protein (Aβ) decomposition, reducing Aβ deposition, reducing damage to nerve cells, improving nerve tissue repair and regeneration capabilities, improving cognitive ability etc. A therapy method using the phototherapy device (100) or the phototherapy instrument (500), and a computer readable recording medium controlling required near infrared light.

A vaporizer device (100) may be configured to adjust, based on ambient pressure, a setpoint temperature and/or a ramp rate of the vaporizer device. The setpoint temperature of the vaporizer device may be adjusted based on the ambient pressure in order to account for differences in the boiling point of a vaporizable material at different ambient pressures. Adjusting the setpoint temperature of the vaporizer device based on ambient pressure may further compensate for changes in the sensitivity of a user's taste buds in different ambient pressure and/or humidity environments. The ramp rate of the vaporizer device may be adjusted based on the ambient pressure such that the vaporizer device is able to achieve the higher boiling point of the vaporizable material in a higher ambient pressure environment in a same quantity of time as a lower boiling point of the vaporizable material in a lower ambient pressure environment.

Systems and methods for delayed delivery of a drug are disclosed. A drug delivery system may include a delivery member for insertion into a patient and a reservoir configured to receive a volume of a drug. An energy source may be activatable by the patient to actuate the reservoir to deliver the drug to the patient as a single bolus. A lockout system may be configured to have a locked state, wherein the lockout system prevents movement of the delivery member and/or activation of the energy source, and an unlocked state, wherein the lockout system permits movement of the delivery member and/or activation of the energy source. The lockout system may be configured to automatically change from the locked state to the unlocked state after a preselected time period has elapsed. An output element may generate a detectable output after the preselected time period has elapsed for notifying the patient.

The present disclosure relates to aerosol delivery devices. In various implementations, the aerosol delivery devices comprise a control device that includes a battery, a control component, and an outer housing that defines receiving chamber, and a cartridge that includes a mouthpiece portion, a tank that contains a liquid composition, and a heater configured to heat the liquid composition. The cartridge and the control device each include at least one connector configured to provide a magnetic and an electrical connection between the cartridge and the control device such that the cartridge can be removably and operatively received into the cartridge receiving chamber of the control body, wherein the at least one connector of the cartridge is located on the mouthpiece portion.

An endotracheal tube includes a main tubular portion including a distal end and a proximal end opposite the distal end, the main tubular portion including a central lumen at least in part defined by a wall of the main tubular portion; a wire lumen disposed within the wall of the main tubular portion, the wire lumen defined at least in part by a sidewall portion of the wire lumen and extending from about the proximal end of the main tubular portion to about the distal end of the main tubular portion; a wire disposed in the wire lumen; and one or more cutouts extending along a portion of the wall of the main tubular portion, the cutouts comprising openings in the sidewall portion of the wire lumen, wherein the cutouts are not in fluid communication with the central lumen.