An apparatus having an adjustable ambient air-oxygen blender that adjustably mixes ambient air with an oxygen supply, especially where a size, diameter or flow rate of an orifice is mechanically adjustable so as to control a quantitative mixing function of the blender.

An apparatus (1) for supplying a gas mixture to a patient, having a gas inlet line (30) with a gas inlet orifice (30a) that splits into a first gas line (31) and a second gas line (32); at least one permeation module (33) arranged on the second gas line (32), the said permeation module (33) having a feed port (33a) in fluidic communication with the second gas line (32), a retentate port (33b) and a permeate port (33c); a third gas line (34) in fluidic communication with the retentate port (33b) of the permeation module (33); a fourth gas line (35) in fluidic communication with the permeate port (33c) of the permeation module (33), and coupling fluidically to the said first gas line (31); and a source (360) of air in fluidic communication with the first gas line (31) and the fourth gas line (35).

A reusable, elastomeric respirator and ventilator, with filter inserts, including a mask body having a pliant facial interface on the interior of the mask body, and two apertures centrally positioned on the front face of the mask body. Two interchangeable plugs or ports are provided to be received within and seal the apertures, deliver oxygen into the mask, or deliver liquids to a wearer of the mask. On opposing sides of the mask body are air filter housings which support an air filter, each air filter housing including a base support structure affixed to the mask body and a top securing structure removably secured to the base support structure. One or more straps are affixed to the mask body to secure the mask body about a wearer's head.

A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the respiratory gas is controlled by a microprocessor, a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway, a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway, and a heated delivery conduit for minimizing condensation of humidified respiratory gas.

A nasogastric tube connector device includes an annular connector body for detachably engaging a through hole of a respirator mask having an inner peripheral surface defining a space, and a fixed member having a first concave surface and two side surfaces cooperating with the inner peripheral surface to define an opening of the space for passing of a nasogastric tube therethrough. A first plug member is detachably inserted through the opening into the space, and includes a second concave surface cooperating with the first concave surface to define a main tube hole communicating with the space. A second plug member is detachably inserted into the main tube hole to sealingly close the opening.

A ventilator includes a bidirectional breath detection airline and a flow outlet airline. The flow outlet airline includes an airline outlet. The flow outlet airline is configured to be connected to an invasive ventilator circuit or a noninvasive ventilator circuit. The breath detection airline includes airline inlet. The airline inlet is separated from the airline outlet of the flow outlet airline. The ventilator further includes a pressure sensor in direct fluid communication with the breath detection airline. The pressure sensor is configured to measure breathing pressure from the user and generate sensor data indicative of breathing by the user. The ventilator further includes a controller in electronic communication with the pressure sensor. The controller is programmed to detect the breathing by the user based on the sensor data received from the pressure sensor.

Provided are a method for controlling oxygen-containing gas output by an oxygen provider, The method includes: acquiring a first pressure measurement of the oxygen-containing gas at the oxygen provider side; determining a pressure estimation of the oxygen-containing gas at the patient side based on the first pressure measurement, wherein the oxygen-containing gas experiences a pressure drop on the gas pathway to arrive at the patient side; and controlling a target parameter of the oxygen-containing gas output by the oxygen provider based on the pressure estimation. With the method or device for controlling oxygen-containing gas output by an oxygen provider, an automated solution to control the oxygen-containing gas based on a pressure measurement at the oxygen provider side is provided, and the complexity of a medical device for oxygen therapy is reduced.

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 humidification of air to be delivered to a patient's airways may include a reservoir, and a humidifier chamber. The humidifier chamber may include a humidifier wick and a heating element for heating the humidifier chamber. The humidifier wick may comprise a fibrous sheet material. The humidifier chamber and wick may be vertically oriented in use such that a first end of the wick is above the second end of the wick. A deioniser may be provided to deionise the liquid prior to the humidifier wick. The apparatus may pasteurise liquid to be delivered to the humidification wick.

The present invention relates to the art of automatic regulation of pulmonary devices for imitating, assisting and/or enforcing the breathing process by converting Bag-Valve-Mask (BVM) or a similar device to enhance both phases of breathing: inhalation and exhalation while applying a variable pressure during the breathing process. It also replaces a mechanical chest compression to the sternum area for automatic pneumatic compression, and it could be complimented with the use of a Tens unit, can be used for extended period of time with a high level of reliability, simplicity, efficacy and low cost. The unique filtration system's goal in this invention is safety of the treating patient as well as assisting personnel. This portable and light device is recommended to be used as a resuscitator for the patients with mild to extremely suppressed or without respiratory drive. The source of power can be electrical, battery operated, manual or a combination thereof.