A blower includes a rotor, a motor adapted to drive the rotor, at least one bearing to rotatably support the rotor, a stationary component, and a bearing sleeve provided to the stationary component. The bearing sleeve is structured and arranged to support and retain the bearing to the stationary component. The bearing sleeve comprises an elastomeric material, and the bearing sleeve comprises one or more bumps or ribs configured to engage along an outer ace of the bearing.

A respiratory therapy device comprising at least one fan unit for generating a respiratory airflow for carrying out respiratory therapy. The fan unit comprises a housing and at least one fan wheel rotatably mounted in the housing. Respiratory air is transported through a channel formed inside the housing, which housing comprises at least one structural element, which reduces the sound emission.

A ventilator includes a ventilation body, the ventilation body includes a ventilation cavity and an air inlet end and an air outlet end communicating with the ventilation cavity, the ventilation body further includes an annular shell configured to form the ventilation cavity, the annular shell is formed with an annular cavity inside, an air inlet and an air outlet communicating with the annular cavity are disposed on the annular shell, the air outlet is communicated with the annular cavity and the ventilation cavity, the air outlet has a slit shape extending along a circumferential direction of the annular shell and is disposed to be capable to guide gas flows out towards the air outlet end. The ventilator may greatly increase the ventilation volume and the gas pressure, by using the ventilation body as mentioned above.

A hand stimulation device that includes a housing defining an interior plenum and having a top portion and a bottom portion; a pair of drive electrodes structured and arranged in a first region of the top portion; a pair of sense electrodes structured and arranged in a second region of the top portion; a processing device disposed within the interior plenum and in communication with each of the pair of drive electrodes and the pair of sense electrodes; at least one sensing device adapted to measure and collect biometric data about the user; and at least one motor that is adapted to generate at least one of tactile feedback and a haptic pattern to a user.

An apparatus is provided to change the absolute humidity of a flow of air for delivery to an entrance of the airways of a patient, the change being compared to the absolute humidity of ambient air. The apparatus has a reservoir configured to hold a volume of liquid. A heating element creates vapour from the liquid. A chamber is provided to mix the flow of air with the vapour. The apparatus has a body having a first wall structure with a chamber inlet port. A closure element having an air inlet port for pneumatically connecting to a source of the flow of air is secured to the body to provide a sealed gas flow path between the air inlet port and the chamber inlet port, and a liquid trap in the gas flow path.

A method for determining that a patient interface component comprising a vent has been replaced between therapy sessions of treatment of sleep disordered breathing, the method comprising: acquiring or receiving first vent flow rate data representing one or more estimated first vent flow rates of gas through a first vent of a patient interface in use during a first therapy session; acquiring or receiving second vent flow rate data representing one or more estimated second vent flow rates of gas through a second vent of a patient interface in use during a second therapy session after the first therapy session; and identifying, by comparison of the second vent flow rate data to the first vent flow rate data, a difference in resistance to flow through the first vent than through the second vent indicating that the second vent is not the same vent as the first vent.

A patient interface assembly includes a flexible cushion configured to sealingly engage the patient's nares and a frame with a pair of flexible extending members that extend laterally from opposite sides of the frame. The frame and the flexible cushion together form a chamber. The patient interface assembly also includes a positioning and stabilising structure configured to maintain the flexible cushion in engagement with the patient's nares. The positioning and stabilizing structure has a pair of headgear straps. Each headgear strap is connected to a respective one of the flexible extending members. The flexible extending members do not form an airflow path for the breathable gas. The headgear straps have a multi-layered structure, at least one layer being made of fabric and at least one layer being made of plastic. In addition, the at least one plastic layer is a rigidizer that adds rigidity to the respective headgear strap.

A system for providing continuous positive air pressure therapy is provided. The system includes a flow generator, a sensor, and a computing device. The computing device is configured to control operation of the flow generator based on sensor data. The computing device is further configured to display, on a display device, one or more questions relating to demographic and/or subjective feedback; responsive to displaying the one or more questions, receive one or more inputs indicating answers to the one or more questions; transmit the answers to a remote processing system; receive, from the remote processing system, settings determined based on the transmitted answers; and adjust control settings of the system based on the received settings.

An apparatus for humidifying a flow of breathable gas includes a water reservoir and a water reservoir dock forming a cavity structured and arranged to receive the water reservoir in an operative position. The water reservoir comprises a reservoir base including a cavity structured to hold a volume of water, the reservoir base including a main body and a thermally conductive portion provided to the main body. The thermally conductive portion comprises a combined layered arrangement including a metal plate and a thin film, the thin film comprising a non-metallic material and including a wall thickness of less than about 1 mm. The thin film is adapted to form at least a bottom interior surface of the water reservoir exposed to the volume of water, and the metal plate is adapted to form a bottom exterior surface of the water reservoir.

A patient interface is configured to deliver a pressurized flow of respiratory gas to a patient's airways. The patient interface includes a cradle base configured to cradle the patients nose in use. Two protrusions extend from the cradle base and are configured to be inserted into the patients nares in use. Each of the protrusions have formed therein an opening configured to allow a continuous flow of air therethrough. In addition, a plenum base forms a plenum chamber together with the cradle base. The cradle base is configured so that movement of the cradle base is decoupled from the plenum base.