A head-mountable flow generator is configured to deliver a flow of breathable gas at a continuously positive pressure with respect to ambient air pressure to a patient interface in communication with an entrance to a patient's airways including at least an entrance of the patient's nares, while the patient is sleeping, to ameliorate sleep disordered breathing. The flow generator includes a motor, an impeller assembly and housing that encases the motor and the impeller assembly. The housing is configured to be mounted on the patient's head and comprises an inlet to receive the flow of breathable gas and a pair of opposing outlets to deliver the flow of breathable gas. In addition, the impeller assembly is configured to pressurize the flow of breathable gas received from the inlet, and the housing is configured to convey the pressurized flow of breathable gas through both outlets.

A patient interface for delivering breathable gas to a patient includes a sealing portion adapted to form a seal with the patient and a support portion to which the sealing portion is mounted. A first headgear chord is connected to a first side of the support portion, and a second headgear chord connected to a second side of the support portion. Headgear is adapted to connect to the first and second headgear chords to secure the support portion to a head of the patient. At least one adjustment device on the support portion is adapted to selectively move the first and second headgear chords to tighten or loosen the headgear.

An infectious aerosol capture mask (IACM) includes a face tent coupled to a suction tube adapter. The face tent includes a proximal opening configured to be disposed over the mouth and nose of a patient. The face tent further includes a distal opening with a smaller diameter than the proximal opening. A coupler is configured to secure the suction tube adapter to the distal opening of the face tent. The suction tube adapter includes a suction port configured to be coupled to a suction tube for active capture of infectious aerosol and left unconnected for passive capture of infectious aerosol. A viral filter is disposed between the suction port and the face tent to capture infectious aerosols expelled by the patient. The IACM further includes one or more one-way valves that are configured to permit airflow into the face tent.

The present invention provides a respiratory mask comprising a nose cushion assembly. The nose cushion assembly comprises a base body and a buffering piece. The base body has a base intake portion, a base connection portion, and an air routing piece disposed at the inside of the base body and having a partitioning wall and a wall connection piece. The inside of the partitioning wall encloses an air intake zone. The wall connection piece is disposed outside the partitioning wall and connects with the base intake portion. Between the partitioning wall and the base intake portion there is defined an air outtake zone. The air intake zone is approximately at the center of the base intake portion. The buffering piece connects with the base connection portion and encloses a nose containing room, which in turn connects with the inside of the base body.

A headgear assembly includes a strap of a first flexible material with an elongate edge, and a second flexible material folded around and running along the elongate edge. The second flexible material may be an elastic material. The second flexible material may also cover an intersection or joint in the first flexible material such that the first flexible material may be made from two flexible materials layered together or joined end to end.

A manually operable valve for restricting airflow to and/or from a patient. The valve includes a body having one or more walls that extend between a first end and a second end. The one or more walls form a passage between the first end and the second end of the body. Two moveable members are positioned on opposing sides of the passage and axially fixed between the first end and the second end of the body. The two moveable members are configured such that depressing the two moveable members inwardly deforms the one or more walls to thereby restrict the passage. When the two moveable members are subsequently released, the one or more walls return to unrestrict the passage.

A connection device and process connect a patient-side coupling unit to a source/sink of a gas including oxygen. The connection device includes a valve device with a first valve (40.1) and with a second valve (40.2). A source-side fluid guide unit establishes a fluid connection between the source or the sink and the valve device. A patient-side fluid guide unit establishes a fluid connection between the patient-side coupling unit and the valve device. The valves are connected in parallel and are arranged between the two fluid guide units. A gas flows from the source through the first and/or second valve to the patient-side coupling unit or through the first and/or second valves to the sink. A control pressure is set at each valve. As a result, the time course of the volume flow downstream of the valve device follows a predefined time course.

An apparatus for controlling the flow of oxygen to a patient comprises an outer housing extending between first and second ends having a passage therethrough. The housing composes a first portion extending from the first end towards the second end and a second portion extending from the second end towards the first end wherein the second portion is threadably rotatable relative to the first portion so as to longitudinally displaced relative to the first portion under rotation thereof so as to adjust at least a portion of the passage extending therethrough adjusting a flow capacity of the passage. The apparatus further comprises connectors at each of the first and second ends operable to connect to oxygen conduits to fluidically conned the oxygen conduits to the passage through the housing.

In an embodiment, a connector or connector assembly for attaching a nasal cannula with a gas delivery hose includes a sensor port for a sensor probe positioned near an end of a nasal cannula, which can allow the sensor probe to be placed closer to the patient's nostrils than previous connector parts allowed. The connector can be configured to advantageously allow the nasal cannula to rotate relative to the gas delivery hose, thereby allowing a patient or healthcare provider to untangle or otherwise straighten the hose or the cannula. The connector assembly can be configured to automatically align locking protrusions on a first component with locking recesses on a second component, where insertion of the second component within the first component causes the second component to rotate relative to the first component, thereby aligning the locking protrusions with associated locking recesses.

Disclosed are an apparatus, system, a kit and a method for delivering supplemental oxygen together with an aromatherapy active. The system comprises one or more oxygen containers for delivering of supplemental oxygen comprising between 35 and 40 percent oxygen—to a user. The system comprise one or more selectable aromatherapy pods, which may be incorporated into the supplemental oxygen delivery system to increase user satisfaction and promote the frequent use of the supplemental oxygen therapy to improve athletic performance.