A respiratory acoustic device is provided that is easy to operate and transport. The device delivers vibrations artificially to the lungs and airways to fluidize mucus adhering to the airways and promote its discharge. A respiratory acoustic device 1 is provided with a housing 10, and a mouthpiece 20 that is in communication with the housing 10. The housing 10 has a reflecting end 12 for reflecting air that has been blown in from the mouthpiece 20 and an open end 13 through which air that has been blown in from the mouthpiece 20 can escape. If a sudden exhalation such as a cough is blown into the housing 10 through the mouthpiece 20, the device causes the noise due to said exhalation to resonate with the oral and lower airway cavities, and vibrate the user's lungs and airways with the low frequency acoustic shock waves generated therein.

A CPAP system for respiratory therapy includes an RPT device configured to supply a flow of gas at a therapeutic pressure, a patient interface, an air delivery conduit configured to pass the flow of gas from the RPT device to the patient interface, and a vent assembly configured to provide a vent flow of gas to discharge gas exhaled by the patient from a pressurized volume to ambient. The vent assembly includes a base including at least one first orifice to allow gas to be discharged along a primary vent flow path and at least one second orifice to allow gas to be discharged along a secondary vent flow path, a diffusing member provided to the base, and a membrane provided to the base. The membrane is configured to apportion the vent flow of gas along the primary vent flow path and the secondary vent flow path throughout respiratory therapy.

A self-administered oxygenation apparatus for increasing pressure within a non-intubated patient's lungs and thereby increasing an amount of oxygen in the non-intubated patient's blood when operated by the patient includes a mouthpiece, a vent member, a resistance member, and a plurality of medical sensors. The medical sensors are configured to receive a portion of the exhalation and to transmit generated medical data to a remote location, such as to a software application via the internet. The mouthpiece includes an external portion through which the patient inhales and exhales. The resistance member is a PEEP valve configured to open upon inhalation so as to allow ambient air inhaled by the patient to pass thereby without resistance and to close upon exhalation, exhalation causing an end shield to pivot outwardly from the vent member under a bias of external elastic members.

A respiratory treatment device comprising at least one chamber, a chamber inlet configured to receive exhaled air into the at least one chamber, at least one chamber outlet configured to permit exhaled air to exit the at least one chamber, and an exhalation flow path defined between the chamber inlet and the at least one chamber outlet. A restrictor member positioned in the exhalation flow path is moveable between a closed position, where a flow of exhaled air along the exhalation flow path is restricted, and an open position, where the flow of exhaled air along the exhalation flow path is less restricted. A vane in fluid communication with the exhalation flow path is operatively connected to the restrictor member and is configured to reciprocate between a first position and a second position in response to the flow of exhaled air along the exhalation flow path.

A resuscitation training device attaches to an air delivery ventilation device to determine if there is a proper mask seal between a live training subject or a training manikin. A pressure sensor attached to the resuscitation training device provides instant feedback to determine if there is a proper seal. The resuscitation training device includes a tubular member having an air metering orifice in fluid communication with the mask and the pressure sensor.

Oxygen concentrator methods and apparatus estimate sieve bed effective capacity. Estimation applies function(s) to a parameter of a measured pressure-time characteristic of the bed, characteristic of a phase of an adsorption cycle of the concentrator at a predetermined motor speed of its compression system. Estimation may involve operating the concentrator at a predetermined bed pressure and measuring a mass flow of gas entering or exiting the bed, and may use the measured mass flow and one or more functions. Estimation may involve a measured bed exhaust mass flow for a purge phase when bed pressure is regulated to maintain a predetermined target pressure using motor speed adjustment. The estimation may apply exhaust mass flow function(s) to the measured exhaust mass flow. Estimation of the effective capacity may involve applying motor speed function(s) to measured motor speed, such as an adjusted one for regulating canister pressure to achieve a target pressure.

An example aerosol delivery device includes a mouthpiece having an airflow outlet, and an airflow passage extending between an airflow inlet and the airflow outlet. The example aerosol delivery device further includes a housing configured to receive a cartridge that includes an aerosolizable substance and a vapor element configured to heat the aerosolizable substance, and an internal power source configured to provide electrical power. The example aerosol delivery device further includes a controller coupled to the internal power source to receive a portion of the electrical power and configured to, when the cartridge is installed at the housing, cause the vapor element of the cartridge to heat the aerosolizable substance to release an aerosol into the airflow passage during an inhalation through the airflow outlet, and a connector configured to receive power from an external source to recharge the internal power source.

A connector having a connector body with an inlet and an outlet defining a gas flow passage therebetween. The connector body has an overlap portion that is configured to overlap with a portion of a second connector when connected. An access passage extends through the overlap portion to the gas flow passage.

A respiratory training device providing both inspiratory and expiratory functional evaluation and training, as well as independent regulation of both the inspiratory and expiratory airway resistance levels used during training. The respiratory training device also includes data acquisition, recording, storage, retrieval and display functions for airway pressure monitoring data to provide functional evaluation, physiological monitoring, and diagnostic features. The respiratory training device allows the user to easily develop and follow precise and advanced training protocols, and utilize the respiratory device in both the clinical and home setting.

A device for acclimatising at altitude comprising a breathing mask defining a confined air space when it is placed on the face of a user. The mask comprising a suction valve to let the surrounding air enter inside the confined space when breathing in; an expiration valve to let air exit with a determined resistance, so as to create an overpressurisation of air in the confined space, when breathing out; and a sensor to establish information about the pressure of the confined space behind. The acclimatisation device in addition comprises a unit for processing the pressure information configured to establish a breathing characteristic of the user and compare it to at least one target value, in view of recommending to them an adjustment of the breathing mode thereof. A method for functioning this device is also provided.