An integrated oxygen supply device that is configured to generate oxygen continuously and release the oxygen non-continuously is provided. In some embodiments, the oxygen generated by the integrated oxygen supply device is stored in a porous material with the integrated oxygen supply device. The delivery of the oxygen produced by integrated oxygen supply device to a patient, in those embodiments, is controlled. In some embodiments, the control of the delivering oxygen is according one or more breathing patterns. The breathing pattern(s) may or may not be a current breathing pattern of the patient. For example, in one embodiment, the breathing pattern is a predetermined breathing pattern with a specified inspiration period followed by a specified expiration period.

An assembly for conducting respiratory air in a patient ventilation system has a plastic respiratory air tube component for conducting respiratory air. At least one heating wire is used to heat the respiratory air. A plastic connector conducts the respiratory air, is integrally connected to an end portion of the tube component and is used for connection to a further, external respiratory air-conducting component. The connector has a connection piece in which an end portion of the heating wire is electrically contacted to an external supply line. The end portion of the heating wire is routed through a lateral wall of the connector to the connection piece. In the connection piece, a recess for accommodating a protective plastic housing for an electrical contacting portion is provided between the heating wire end section and the end portion of the supply line.

The present invention relates to an apparatus for providing respiratory assistance to a user via a user conduit. The apparatus being operable in a humidifying mode and a non-humidifying mode, and includes a humidification chamber for containing an amount of water that can be located in an operating position in the humidifying mode and, optionally separate from the apparatus in the non-humidifying mode. The apparatus may also have an auxiliary flow path that can be activated in the non-humidifying mode and a powered device that heats water in the humidification chamber when the apparatus is in the humidifying mode.

Methods and apparatus provide controlled operations in an oxygen concentrator (100) such as by adjusting valve opening time to regulate amount of oxygen enriched air released to a user. The apparatus may generate, with a sensor configured to sense pressure at a location associated with accumulation of enriched air produced by the concentrator, a signal representing measured pressure of the accumulated enriched air. The apparatus may generate, with a sensor, a signal indicative of respiration of a user of the concentrator. The apparatus may include a controller configured to receive the measured pressure and respiration signals. The controller may control, responsive to the respiration indication and according to a target duration, actuation of a valve adapted to release a bolus of accumulated oxygen enriched air. The controller may dynamically determine the target duration during the release of the bolus according to a function of a value of the measured pressure.

Embodiments provide an aeromedical bio-containment module for use in a cargo plane. The aeromedical bio-containment module includes a fully integrated pallet system allowing for the module to roll onto the cargo plane. An integrated set of lugs allows the module to be locked into the cargo plane floor without the use of chains or other pallets. The aeromedical bio-containment module features a ward area for safe treatment of patients, an anteroom, and an office area for personnel. The aeromedical bio-containment module operates under a negative pressure system, and includes a full air filtration system to remove pathogens, particulates, and other airborne contaminants.

A reusable, elastomeric respirator and ventilator, with filter inserts, including a mask body having a pliant facial interface on the interior of the mask body, and two apertures centrally positioned on the front face of the mask body. Two interchangeable plugs or ports are provided to be received within and seal the apertures, deliver oxygen into the mask, or deliver liquids to a wearer of the mask. On opposing sides of the mask body are air filter housings which support an air filter, each air filter housing including a base support structure affixed to the mask body and a top securing structure removably secured to the base support structure. One or more straps are affixed to the mask body to secure the mask body about a wearer's head.

A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the respiratory gas is controlled by a microprocessor, a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway, a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway, and a heated delivery conduit for minimizing condensation of humidified respiratory gas.

A nitric oxide delivery system, which includes a gas bottle having nitrogen dioxide in air, converts nitrogen dioxide to nitric oxide and employs a surface-active material, such as silica gel, coated with an aqueous solution of antioxidant, such as ascorbic acid. A nitric oxide delivery system may be used to generate therapeutic gas including nitric oxide for use in delivering the therapeutic gas to a mammal.

A nitric oxide delivery system, which includes a gas bottle having nitrogen dioxide in air, converts nitrogen dioxide to nitric oxide and employs a surface-active material, such as silica gel, coated with an aqueous solution of antioxidant, such as ascorbic acid. A nitric oxide delivery system may be used to generate therapeutic gas including nitric oxide for use in delivering the therapeutic gas to a mammal.

A humidification system can include a heater base, a chamber, and a breathing circuit. The heater base includes a heater plate positioned in a recessed region, and a heat conductive portion of the chamber is configured to contact the heater plate. The heater base includes a guard configured to control movement of the chamber into and out of the recessed region. The guard includes an anti-racking mechanism. The chamber includes an inlet port, an outlet port. A downward extension extends into the chamber from the inlet port, and a baffle is disposed at a lower end of the downward extension. A component of the breathing circuit can include a conduit hanging end cap for shipping and storage. The end cap can include a hanging component to allow the breathing circuit component to be hung from a medical stand. The system can detect when breathing circuits are connected in reverse.