Abstract: A pneumatic system for delivering oxygen to a subject, including an oxygen supply channel having an inlet, a patient delivery outlet and an exhaust; and a flow control element configured to control the flow from the oxygen inlet to the patient delivery outlet, or to the exhaust; wherein inhalation by the patient causes the flow control element to assume a first position, allowing oxygen to flow from the oxygen inlet to the patient delivery outlet; and wherein exhalation by the patient causes the flow control element to assume a second position, directing oxygen flow from the oxygen inlet to the exhaust.

Abstract: A nozzle for use in delivering a mixture of aerosol propellant and drug formulation. The nozzle includes a drug product inlet configured to receive a mixture of aerosolized propellant and an intranasal dosage form. The inlet is disposed at the proximal end. A nozzle body is secured to the drug product inlet. Two or more channels are disposed within the body. Two or more orifice apertures are disposed at the distal end of the nozzle.

Abstract: A cuff for an air delivery conduit includes a first end portion provided to a tube and a second end portion adapted to engage a tubular connector. The second end portion includes an annular bead for sealing and retention.

Abstract: A protective mask having a valve assembly that allow a user to drink a beverage while wearing the mask to maintain a safe environment by filtering contaminants, such as pathogens and particles from passing through the mask. The valve assembly may be provided on the mask or may be separately provided for attachment to a mask. The protective mask with the valve assembly has an attachment portion that allows common beverage straws to connect with the valve assembly to allow liquids to be draw through the mask by a user through a passageway. A check valve limits liquid flow in a single direction and actuates to open the valve when a user draws in liquid through the mouthpiece. The valve remains closed and blocks passage of inhaled or exhaled air, and blocks liquid flow in the direction opposite of the flow direction.

Abstract: Various embodiments of a respirator (10) that includes a harness (13, 16), a mask body (12), and an exhalation valve (14) are disclosed. The exhalation valve (14) can include a valve seat (20) and a flexible flap (22) that is in engagement with the valve seat. The flexible flap can have one or more materials that can cause the flap to flash (26) when moving from a closed position to an open position or vice versa. The flashing valve can make it easier for a user to ascertain whether the valve is operating properly.

Abstract: A patient interface for sealed delivery of a flow of air at a continuously positive pressure with respect to ambient air pressure to an entrance to the patient's airways including at least entrance of a patient's nares to ameliorate sleep disordered breathing may include a seal-forming structure comprising a foam undercushion and a textile membrane for contact with the patient's face; a positioning and stabilising structure to maintain the seal-forming structure in sealing contact with an area surrounding an entrance to the patient's airways while maintaining a therapeutic pressure at the entrance to the patient's airways; and a plenum chamber pressurised at a pressure above ambient pressure in use.

Abstract: A respirator system is disclosed that includes a foldable head cover assembly including a face seal portion. The respirator assembly further includes a visor assembly attached to the head cover assembly and a head suspension system removably attached to the visor assembly. The visor assembly and the head cover assembly on one hand, and the suspension system on the other, are separable and foldable to enable storing and/or shipping the same separately. A head suspension system is also disclosed.

Abstract: A system and method for providing ventilatory support to a patient suffering from sleep disordered breathing (SDB), in particular, non-obstructive SDB, such as Cheyne Stokes respiration and hypoventilation, including obesity hypoventilation syndrome. The system and method monitor obtain data corresponding to a breathing pattern of a patient and determine when the patient experiences oscillating breathing or low spontaneous ventilation. In particular, the system and method determine when the patient's real-time breathing patterns fall below a predetermined baseline threshold, and subsequently initiate a short series of mechanical breaths to be delivered to the patient.

Abstract: A gases delivery system for medical use is disclosed that has a container configured to house a metal-organic framework material within at least one section of the container. An activation mechanism may be associated with the container. The metal-organic framework material may contain one or more substances such that the one or more substances may be released from the metal-organic framework material when energy is applied to the container via the activation mechanism. The activation mechanism may be a heating mechanism. One or more containers housing metal-organic framework materials may be used in a gases recirculation system.

Abstract: A type flavor inhaler (100) comprises aerosol flow passage (140) guiding aerosol generated by the atomization unit (111) to the mouthpiece side. The aerosol flow passage (140) includes: a first flow passage (140A) which guides aerosol to the mouthpiece side through the flavor source (132); and a second flow passage (140B) which is different from the first flow passage (140A). An aerosol reduction rate of the second flow passage (140B) is smaller than an aerosol reduction rate of the first flow passage (140A).

Abstract: A ventilator (100) configured to control a pressure and gas mixture for an air flow. The ventilator include: a gas source (220); a proportional valve (210) configured to control a gas flow rate from the gas source; a mix controller (170) in communication with the proportional valve, the mix controller configured to monitor a flow of gas through the blower, and further configured to control a percentage of oxygen in the output flow; a blower motor (160); and a blower motor controller (162) configured to control a speed of the blower motor using a current feedback loop, a blower speed feedback loop, a flow feedback loop, and a pressure feedback loop. The ventilator can also include, for example, a pseudo-derivative feedback compensator, a complimentary filter, and/or a speed controller.

Abstract: An ultrasonic nebulizer includes a tank unit configured to be detachable with respect to a main body. The tank unit includes a working tank in which an ultrasonic vibrator is incorporated, a medicine tank, and a medicine tank cover, which are arranged overlaid in the stated order. The output of an oscillation circuit in the main body is applied to the ultrasonic vibrator through a main body-side contact electrode and a tank-side contact electrode when the tank unit is mounted on the main body. The main body includes an air fan that blows air into the medicine tank through an air duct of the medicine tank cover, and a medicine tank cover detection unit that detects whether or not the air duct of the medicine tank cover is adjacent to the main body so as to detect whether or not the tank unit is mounted on the main body.

Abstract: A flow of breathable gas is delivered to a subject through a patient interface assembly. An enhanced technique for determining whether the airway of subject is disengaged from the patient interface assembly. A model that provides predicted values of a dynamic property of the flow of breathable gas is fit to measured values of the dynamic property. The model and/or the fit of the predicted values to the measured values are then analyzed to determine whether or not the airway of the subject is disengaged from the patient interface assembly. This provide enhanced determination of these conditions even in implementations in which a restrictive patient interface assembly is used.

Abstract: A patient interface for sealed delivery of a flow of air to ameliorate sleep disordered breathing may include: a seal-forming structure to form a pneumatic seal with the entrance to the patient's airways; a positioning and stabilising structure to maintain the seal-forming structure in sealing contact with an area surrounding the entrance to the patient's airways; a plenum chamber pressurised at a pressure above ambient pressure in use; a connection port for the delivery of the flow of breathable gas into the patient interface; and a device positioned within a breathing chamber defined, at least in part, by the seal-forming structure and the plenum chamber, wherein the device divides the breathing chamber into a posterior chamber and an anterior chamber, and wherein the device comprises a plurality of apertures such that turbulence of the air in the posterior chamber is less than turbulence in the air in the anterior chamber.

Abstract: A humidifier for an airway pressure support system, includes a base, a number of side walls extending from the base, and a top wall provided opposite the base, wherein the base, the number of side walls, and the top wall are made from an elastomeric material and at least partially define an internal chamber for receiving and holding a liquid. The humidifier also includes a plurality of support structures provided on or within the humidifier, each support structure extending along at least the number of side walls, wherein the humidifier is structured to collapse from an initial, expanded condition to a collapsed condition when a compressive force is applied to the top wall in the initial, expanded condition and to automatically return to the initial, expanded condition when the force is removed.

Abstract: A respiratory apparatus includes components to protect operations of the apparatus. For example, in some versions, the apparatus may include a power supply, a motor powered by the power supply, and a transient absorption diode circuit between the motor and the power supply. The transient absorption diode circuit may be configured to absorb energy generated by the motor from rotational kinetic energy. Such absorption may serve to protect the components of the apparatus. In some examples, the apparatus may include a fault mitigation integrated circuit (IC). The IC circuit may be included in the respiratory apparatus to detect one or more faults based on physical and system parameters of the apparatus. The fault mitigation integrated circuit may generate a signal to stop the motor based on the detected fault, and may digitally communicate with a processor information about the detected fault.

Abstract: A cartridge for an aerosol-generating system may include a first chamber housing defining a first chamber and a second chamber housing defining a second chamber that is separate from the first chamber. The first chamber may contain an aerosol-forming substrate in the form of a gel, and the second chamber may contain a source of a desired compound. The first and second chamber housings may be separate or separable structures.

Abstract: One aspect of the present disclosure relates to a reversible airway device. The reversible airway device (10) can include: a supra-glottic airway support (12) comprising a multi-lumen tubular guide (14) and an optional sealing member (16); an endotracheal tube (26); and at least one seal (42). The multi-lumen tubular guide has a distal end portion (18), a proximal end portion (22), a first passageway (20) extending between the distal and proximal end portions, and a second passageway (24) that is non-concentric with the first passageway and also extends between the distal and proximal end portions. The at least one seal is disposed within the first passageway, the second passageway, or both, so as to occlude the flow of a gas through the first passageway and/or the second passageway. The endotracheal tube can be inserted into the first or second passageway and can traverse the seal.

Abstract: An aerosol-generating system may include an electrical power supply, an electrical heater connected to the electrical power supply, and a substrate container. The substrate container may define a blind cavity containing an aerosol-forming substrate in the form of a gel that is a solid at room temperature. The electrical heater is external to the substrate container and configured to heat the substrate container to generate a vapor without contacting the aerosol-forming substrate. As result, the possibility of unwanted materials building up on the electrical heater can be reduced, thereby providing a more reliable and consistent performance.

Abstract: The present invention relates to a respiratory tubing set for controlling breathing of a patient. A tubing set for controlling breathing of a patient includes a respiratory conduit. The respiratory conduit is configured to be coupled to a patient interface device and is further configured to be coupled to a pressurized air generating device. The respiratory conduit includes at least two airflow control devices, positioned between the patient interface device and the pressurized air generating device that cooperate to closely control the CO2 levels in the patient's bloodstream through the control of the patient's respiration.