Systems and methods are provided for portable and compact nitric oxide (NO) generation that can be embedded into other therapeutic devices or used alone. In some embodiments, an ambulatory NO generation system can be comprised of a controller and disposable cartridge. The cartridge can contain filters and scavengers for preparing the gas used for NO generation and for scrubbing output gases prior to patient inhalation. The system can utilize an oxygen concentrator to increase nitric oxide production and compliment oxygen generator activity as an independent device. The system can also include a high voltage electrode assembly that is easily assembled and installed. Various nitric oxide delivery methods are provided, including the use of a nasal cannula.

A water reservoir for use with a respiratory pressure therapy (RPT) device includes a water reservoir base configured to hold a volume of water to be used for humidification of pressurized breathable air, the water reservoir base including a conductor plate constructed from a heat conducting material; a water reservoir lid connected to the water reservoir base, wherein the water reservoir lid and the water reservoir base are connected via a pair of joints positioned proximate a first end of the water reservoir; a retainer configured to secure the water reservoir to the water reservoir dock; a latch that secures the water reservoir lid and the water reservoir base, the latch being positioned on the water reservoir proximate a second end that is opposite to the first end; and a water reservoir inlet and a water reservoir outlet positioned on a common side of the water reservoir so as to face a common direction.

An apparatus for generating and providing a pressurized breathable gas to a patient's airways includes a respiratory pressure therapy (RPT) device having an engagement port pneumatically and electrically coupled to the RPT device, and an air delivery tube configured to engage the engagement port so as to pass a flow of breathable gas to a patient interface. The air delivery tube includes electric contacts associated with a heating and/or a sensing arrangement. The air delivery tube includes a locking collar rotatably movable between (1) an unlocked position to allow connection/disconnection of the air delivery tube to/from the engagement port, and (2) a locked position to releasably lock the air delivery tube to the engagement port. The air delivery tube is structured and arranged to, when the locking collar is rotated into the locked position, pneumatically connect to the engagement port and define an operational configuration of the apparatus.

A medical tube transports gases to and/or from a patient. The medical tube includes a bead wrapped around a longitudinal axis of the medical tube. The bead forms a first portion of a lumen wall of the medical tube. The medical tube also includes a film wrapped around the longitudinal axis of the medical tube. A first portion of the film overlies the bead, and a second portion of the film forms a second portion of the lumen wall. The lumen wall, formed by the bead and the second portion of the film forms a substantially smooth bore. The medical tube can be reusable or reprocessable.

The invention relates to a respiratory system comprising a first patient interface for delivery of a first flow of gases to a patient, a second patient interface for delivery of a second flow of gases to the patient, and a device and/or sensing arrangement that is configure to facilitate a switching of the system between a first respiratory mode where the device allowing delivery of the first flow of gases to an outlet of the first patient interface when the second patient interface is absent from the patient, and a second respiratory mode where the device reducing or stopping delivery of the first flow of gases to the outlet of the first patient interface when the second patient interface is located together with the first patient interface upon the patient.

A system and method of use for an operational halotherapy device and red light device in an enclosed space. The halotherapy and red light system generally comprise a machine disposed in the enclosed space that disperses salt particles into the air, and includes a red light device that emits red light waves. The combination of both devices produces a refractory phenomenon when the red light waves make contact with the salt particles dispersed in the air to cause a plethora of multi-dimensional dispersions of light waves. Moreover, every time a salt particle makes contact with a red light wave, a portion of the wave light is absorbed by the particle and its temperature increases, lessening the moisture in the particle. The lessening of moisture in the particle dries the particle further, which enhances the therapeutic properties of the inhalable salt particle.

A device for monitoring use of an inhaler, including a main module for coupling to an inhaler, having a body accommodating operating modules and having a pivotable arm with a proximity sensor for measuring a distance between an element of the inhaler and the proximity sensor, and a microcontroller for receiving measurements of the distance from the sensor and for determining when the device was used based on the measurements of the distance received from the sensor.

A ventilator system includes inspiratory lumen(s) and expiratory lumen(s). Inspiratory lumen(s) provide inspiratory gas mixtures to patient's airways, for instance with separate inspiratory lumens providing inspiratory gas(es) to separate airways portions (e.g., separate lungs, bronchi, lobes). Expiratory lumen(s) evacuate expiratory gases from airways, for instance with separate expiratory lumens evacuating gases from separate airway portions. Separate lumen(s) for separate portions of airways functionally separates structural airway portions, and allows maintenance of near-continuous flow across the respiratory cycle. This can reduce dead space and clear disease-causative agent(s) suspended therein, improving outcomes and reducing cross-contamination between airway portions. The system allows for independent titration of PEEP, pCO.sub.2 and/or pO.sub.2 without permissive hypercapnia. The system can include PEEP protection mechanisms, enhanced suctioning, suctioning mode(s), real-time compliance measurements, automatic settings choice to operate within highest lungs compliance, improved tube and lumen airway insertion, threading lumens, mounting device(s) for threaded lumens, etc.

A gas filter device for a medical device that provides a gas to a patient including first and second gas filter elements; a body defining a cavity receives the first and second gas filter elements in series and spaced apart from, each other; first and second end walls at opposites ends of the cavity; a first coupler extending from the first end wall; a second coupler extending from the second end wall, wherein the first coupler and the second coupler define a flow channel in communication with the cavity.

A moisture exchange fabric is disclosed the fabric comprising: a substrate fabric; a polymer having lower critical solution temperature (LCST) of between 25 C. and 39 C. bonded to the substrate fabric; and a filament sewed into the substrate fabric. Also disclosed is a humidifying apparatus using the moisture exchange fabric.