An apparatus for delivering a flow of gas has a housing, a cover, and a magnetic coupling system arranged to magnetically couple the cover—to the housing. Each of the housing and cover having complementary locating features, the locating features being adapted to locate and align the cover and the apparatus relative to each other to allow for the magnetic coupling. The apparatus also has a handle movably connected to the housing and is movable from a first position to a second position. The housing and the handle comprise complementary interlock features arranged to engage with each other when upward force is applied to the handle in the second position, and the interlock features are disengaged from each other when the handle is in the second position but upward force is not applied to the handle.

An apparatus or kit for a respiratory support system for delivering humidified gas to a user or patient. The apparatus comprising a humidifier chamber in pneumatic communication with a gases source, an inspiratory conduit in pneumatic communication with the humidifier chamber downstream of the humidifier chamber, a filter that is in pneumatic communication with the inspiratory conduit downstream of the inspiratory conduit, and a patient interface for delivering humidified gas to a user or patient, wherein the patient interface is in pneumatic communication with the filter downstream of the filter, or is configured to be placed in pneumatic communication with the filter downstream of the filter.

Described herein are improved assisted ventilation interfaces along with methods and uses thereof. The interfaces comprises a hood embodiment with altered design aspects to decrease or even avoid the risk of leakage and potential viral transmittance along with providing other benefits. In one aspect, the patient interface comprises a hood with a free-breathing valve and an integral viral filter. The free-breathing valve and viral filter may be separate to or integral to the exhaust port. In a further embodiment multiple branches may be used from the exhaust port with multiple viral filters. In a further embodiment, an internal pressure gauge may be used. In a further embodiment dual air sources may be used.

A breath detection apparatus for monitoring individual breaths of a patient. The apparatus includes a sensing assembly comprising a humidity sensor. The sensing assembly adapted to be connected to an oxygenation device wherein respiratory gases of a patient are directed over the sensing assembly and the humidity sensor is adapted to monitor differences in humidity during a breath of the patient. The humidity sensor generates an electrical signal representing a humidity level in response to measuring the humidity during the breath. The apparatus also includes a processor in electrical communication with the sensing assembly to receive electrical signals generated by the humidity sensor and determine a state of the relative humidity during the breath, and a visual display element controlled by the processor and adapted to display a predetermined visual alert in response to the state of the relative humidity during the breath.

Methods and apparatus may implement controlled generation of oxygen enriched air in an oxygen concentrator while implementing control that reduces pneumatic imbalance between the concentrator's canisters, such as dynamic pressure imbalance or other pneumatic characteristic. One or more controllers may regulate operation of a compressor that feeds a pressurised air stream to the concentrator's canisters. This may regulate speed of the compressor to a speed set point for generating the pressurised stream. The regulating may involve generating a compressor control signal having a characteristic parameter such as a power parameter. The controller(s) may operate valve(s) in a cyclic pattern so as to produce oxygen enriched air in an accumulator. A cycle of the cyclic pattern may include a plurality of phases, where each of the plurality of phases has a duration. The controller(s) may then generate a dynamic adjustment to the duration(s) based on an evaluation of the characteristic parameter.

There is provided herein, a bite block (100) comprising an insertion channel (134) and an airway channel (132) wherein the airway channel is adapted to receive exhaled breath and wherein the first insert channel is adapted to pass a medical instrument. There is provided herein, a bite block comprising an oral insert channel, wherein a portion of said channel opens into a cavity (142) adapted to slidably receive an oral prong (270) the oral insert channel is adapted to receive exhaled breath.

An apparatus for determining a respiratory condition, the apparatus includes: a signal acquirer which is configured to acquire a signal waveform corresponding to a respiratory flow of a subject; a differential calculator which is configured to acquire a differential waveform which is obtained by performing differentiation of the signal waveform; and a first determiner which is configured to determine that inspiratory flow limitation occurs in the subject, when the differential waveform satisfies a predetermined condition in a portion of the signal waveform, which corresponds to inspiration of the subject.

A gas delivery conduit adapted for fluidly connecting to a respiratory gases delivery system in a high flow therapy system. In one embodiment, a nasal cannula includes a base portion defining a first therapeutic gas passageway, a nozzle disposed adjacent the base portion and defining a second therapeutic gas passageway, the first passageway being in gaseous communication with the second passageway and a conduit configured to facilitate sensing that has an inlet side that is independent of and axially spaced apart from an outlet side of the nozzle. The conduit inlet side can extend beyond the nozzle outlet side of the nasal cannula. Additionally, the nasal cannula has a feature adapted to prevent one of the conduit and the nozzle from creating a seal with a user's rare and a feature adapted to prevent one of the conduit and the nozzle from creating a seal with a user's nare.

A nasal cannula device includes a cannula body. The cannula body includes an accommodating chamber inside and includes two nasal joint tube extended outwardly and communicating with the accommodating chamber. A junction ring is formed between the cannula body and each nasal joint tube. At least one of the cannula body and each nasal joint tube includes a recessed annular section recessed at one side of each junction ring. The recessed annular section has a thickness smaller than a thickness of the cannula body, a thickness of each nasal joint tube, and a thickness of each junction ring. Accordingly, the nasal cannula device can deliver a therapeutic gas smoothly.

A personal entertainment respiratory apparatus provides air to a user to provide a fully immersive entertainment experience. The personal entertainment system may comprise a flow generator for providing the flow of air. A personal spatial respiratory interface may be coupled to the flow generator. The personal spatial respiratory interface may comprise an outlet for the flow generator. The personal spatial respiratory interface may further be configured to direct the flow of air within an ambient breathing proximity of a user. The personal entertainment respiratory apparatus may further comprise a controller and a sensory particle dispenser. The controller and sensory particle dispenser may be configured to selectively activate release of a sensory particle from the dispenser into the directed flow of air in response to an entertainment triggering signal.