Gas concentrating systems and methods are provided. In one embodiment, a gas concentrating system and method is provided that includes component heat management. The heat management system can include, for example, one or more air cooling paths. The air cooling paths direct cooling air into and out of component spaces having heat-generating mechanisms. In other embodiments, the heat management system can also include component spaces that are insulated against the heat of heat-generating components. By cooling heat-generating components and insulating other components from heat, reduced wear and extended component life can be achieved. This reduces component failure and costly service to repair or replace failed or worn components. Also, gas concentrating systems and methods are provided for mounting system components with or without the use fasteners and in combination with or without component heat management.

Systems and methods for nitric oxide (NO) generation systems are provided. In some embodiments, an NO generation system comprises at least one pair of electrodes configured to generate a product gas containing NO from a flow of a reactant gas. The electrodes have elongated surfaces such that a plasma produced is carried by the flow of the reactant gas and glides along the elongated surfaces from a first end towards a second end of the electrode pair. A controller is configured to regulate the amount of NO in the product gas by the at least one pair of electrodes using one or more parameters as an input to the controller. The one or more parameters include information from a plurality of sensors configured to collect information relating to at least one of the reactant gas, the product gas, and a medical gas into which the product gas flows.

A clear, soft and malleable plastic constructed face mask is provided that has an elastic strap that is used to secure the mask onto a patient's face. The mask comprises of a malleable aluminium strip on the top for easy molding of the mask around the patient's nose; a front opening covered with a paper filter; and two side openings covered with a paper filter. The mask provides supplemental oxygen through connection to a Y-shaped respiratory/ventilator circuit or standard oxygen tubing. The mask also allows the patient to breathe comfortably without a supplemental oxygen source. It has ribbed tubing for gas sampling. The mask allows a health care employee to visualize breathing on the clear plastic material. The mask provides filtration of aerosolized contaminants.

An apparatus used to disinfect viruses/bacteria contaminated exhaust air from devices, such as ventilators, CPAP, APAP, VPAP auto, BiPAO, ECMO, and also devices for air filtration used in cars, buildings, ships, planes, etc. is disclosed in this document. A heat source is used to burn the contaminated air at elevated temperatures, such as 100° C., 500° C., 1,000° C., and/or even more, in a confined environment to inactivate/destroy viruses/bacteria carried in the air. The heat sources can be, but not limited to, electrical, gases, infrared, microwave, and Ultraviolet (UV). After disinfection, the exhaust air from the apparatus is then released to the ambient environment, or to the next chamber for further treatment.

A portable apparatus for oxygen delivery includes a receptacle, a mouthpiece and a tube. In another aspect the mouthpiece includes a first fluid channel for a first fluid and a second fluid channel for a second fluid that is different from the first fluid. In a further aspect, the portable apparatus includes a receptacle, a mouthpiece and a tube in which the mouthpiece includes a teeth engagement portion, a lip engagement portion and a lip protection portion.

Apparatus permit a delivery of a flow of breathable gas to a patient's airways. In one version, a coupler extension may include a seat portion to permit use of a mask with a nasal cannula. In some versions, the coupler extension is configured to conduct the flow of gas to prongs of a nasal cannula. The seat portion can receive and seal with a cushion of a respiratory mask and may have a sealing bevel to promote sealing between the cushion of the respiratory mask and a facial contact surface of a user. In some versions, a nasal interface may include naris pillows to seal with and conduct a flow of breathable gas into a nares of a user. Each naris pillow may include a nasal projection to conduct a further flow of gas. The nasal projection may extend within the naris beyond the seal of the naris pillow.

A pacifier comprising a reusable suction part and at least one exchangeable housing part which are releasably connectable to each other, wherein said suction part comprises a nipple and a shield connected to each other, wherein said suction part comprises a passageway through which a fluid can pass from outside a mouth of a user of the pacifier to inside the mouth of the user of the pacifier, and wherein said suction part comprises at least one first connection device, and wherein said housing part comprises a housing and at least one second connection device which is releasably connectable to the at least one first connection device, wherein said housing comprises at least one heat and moisture exchanger (HME) device and/or at least one filter device.

Provided is a filtering facepiece respirator. The respirator includes a mask body having an anterior side portion, a posterior side portion, a middle portion, a first side portion, a second side portion, a top side portion, a bottom side portion and outer edge portions. The respirator further includes a primary port positioned at the anterior middle portion of the mask body and a detachable primary port adapter which is positioned over and engages the primary port. The respirator may further include an oxygen port and oxygen port adapter and a luer port and luer port adapter.

An isolation hood for respiratory treatment is disclosed. The isolation hood may include a head enclosure defining an interior volume configured to receive the head of a patient, and a neck seal configured to couple the head enclosure to a neck of the patient. The isolation hood may include an inlet port configured to be coupled to a distal end of a treatment source tube and to a first end of a treatment delivery tube, and an outlet port configured to be coupled to an inline particle filter configured to permit air to flow through the head enclosure. The neck seal and the inline particle filter are each configured to prevent viral/bacterial aerosolization outside the hood. The inlet and outlet ports may be attached to respiratory tubing and non-invasive ventilatory equipment to permit aerosol-generating procedures within the hood while preventing viral/bacterial aerosolization outside the hood.

A breathing assistance apparatus is configured with features that improve serviceability of the apparatus. The apparatus can include animations to provide instruction regarding correcting easily-identified fault conditions and to provide instruction regarding routine maintenance routines. The apparatus also can be configured with top level control menus that are obscured in a manner to limit manipulation of the top level control elements by unauthorized users.