A system provides warm, humidified pas to a patient via a patient interface. Horizontal connections can be used between the humidification chamber and conduit. To reduce the likelihood of condensate flowing back to the humidification chamber, or dead space or gases recirculation regions occurring within the gases flow path, a raised portion is positioned inside of the flow path to improve flow characteristics and to provide a barrier for condensate back flow. The raised portion also reduces the amount of condensate that is formed in the system and provides better flow characteristics for sensing purposes.

A cushion/frame assembly for a patient interface includes a cushion frame and a cushion. The cushion frame includes a cushion frame material, an annular wall portion having an opening that extends along a cushion frame longitudinal axis, and a projection extending radially with respect to the opening. The cushion frame is configured to snap fit with an outer frame having headgear attachment points and being configured to engage an inlet conduit. The cushion is connected to the cushion frame. The cushion is structured to form a seal with the patient and includes a cushion material that is more flexible than the cushion frame material.

An oxygen facemask that has pathogen filtering capability can be used in conjunction with a capnometer to measure carbon dioxide levels in a patient. Facemask can be used to provide critical breathing assistance to patients. In certain instances, a patient’s blood CO2 level can be the difference between a good versus a bad outcome. Accordingly, in certain circumstances there is great value in evaluating a patient’s CO2 with a capnometer from breath exiting the facemask, which correlates to CO2 in their blood. Because some of these patients carry airborne transmissible viruses, an exhalent filtration system is envisioned included in the facemask that filters the patient’s breath from those helping the patient in a common space. The exhalent filtration system incorporates both filtering air exiting the facemask directly into a common space and indirectly into the common space by way of the capnometer.

A catheter mount is configured to be attached to a respiratory apparatus. The catheter mount includes a plurality of ports in fluid communication with each other. The plurality of ports include an interface port configured to connect to an interface tube, a conduit port configured to connect to a conduit tube, and at least one suction port configured to allow insertion of a suction catheter. The at least one suction port can be positioned to allow the suction catheter, when inserted, access to both the interface port and conduit port.

A cleaning apparatus for cleaning of medical machine components of machines such as CPAP machines, nebulizers, PEEP machines, and the like is disclosed herein. The cleaning apparatus comprises a container body. A carousel is configured for placement within the container body. The carousel comprises a support structure. The carousel further comprises a helical ramp attached to the support structure and extending helically from an operative top end of the support structure to an operative bottom end of the support structure along a periphery of the support structure.

A capnography system includes a CO.sub.2 sensing system having a CO.sub.2 sensor configured to measure a CO.sub.2 concentration in exhaled breath of a subject, a processor configured to derive one or more breath related parameters based on the measured CO.sub.2 concentration, and a communication unit. The capnography system includes a tubing system configured to allow flow of respiratory gasses therethrough. The tubing system includes a connector configured to connect the tubing system to the CO.sub.2 sensing system and a communication component configured to provide an indication of a type of the tubing system to the communication unit. The communication unit is configured to transfer data to the processor based on the indication obtained from the communication component, and the processor is configured to change or suggest a change of an operation mode of the CO.sub.2 sensing system based on the data.

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 inline muffler for use with a positive airway pressure (PAP) apparatus. The muffler may provide an expansion chamber with baffles that capture acoustic energy using, for instance, a disruptive gas flow path to effectively reduce downstream noise associated with a flow of pressurized gas produced by the PAP apparatus. In some embodiments, the muffler is constructed of two mostly identical halves with baffle segments being integrally formed therewith.

A ventilator that moves breathable air into and out of the lungs of a patient. The ventilator includes an inspiratory circuit with an inlet, a bellows, and an outlet port for moving air into the lungs of the patient. An expiratory circuit includes an inlet port and a discharge port for moving the air out of the lungs. The inspiratory circuit is adjustable to control a number of breathes per time period and a volume of the breaths.

A non-ventilator ET tube cap used to oxygenate a patient during an intubation procedure. The ET tube cap generally comprises an oxygen source connector configured to connect to an oxygen source via an oxygen tube. This provides oxygen to a patient via an ET tube while being intubated. The ET tube cap further includes an ET tube receiving aperture that is specifically arranged to engage an ET tube in a removable relationship prior to the ET tube connected to a ventilator while the ET tube is deployed in a patient. Optionally, the ET tube cap can comprise at least two pressure relief valves that open when pressure inside of the ET tube cap exceeds a predetermined pressure threshold to prevent harm to the patient that is being intubated.