Abstract: A patient interface device is for a pressure support system that includes a flow generator that produces a flow of breathing gas to be delivered to an airway of a patient. The patient interface device includes a sealing element to engage a face of the patient and receive the flow of breathing gas; a lumen having a first end and a second end opposite and distal the first end, the first end being in fluid communication with an interior of the sealing element; a connector member coupled to the second end of the lumen; a pressure sensor coupled to the connector member, the pressure sensor sensing pressure of a gas exiting the second end of the lumen; and a surface provided on one of the lumen and the connector member, the surface defining a thru hole through which undesirable liquid in the lumen can escape.

Abstract: A respiratory interface system for use in delivering a flow of a positive pressure breathing gas to an airway of a patient includes a patient interface device. The patient interface device includes a tubing assembly for positioning on the head of the patient, a mask having a sealing element for sealingly engaging about the airway of the patient, and an adaptor. The mask is coupled to the tubing assembly via the adaptor, and the tubing assembly, the mask, and the adapter define a pathway for conducting the flow of the positive pressure breathing gas to the airway of the patient.

Abstract: A pressure generating device structured to be operatively coupled to a system for delivering a flow of pressurized breathing gas to a patient includes a controller and a touch screen with a graphical user interface (GUI). The system comprises a number of accessory components, and the controller is structured to monitor a number of factors related to determining when the pressure generating device and each of the number of accessory components should be replaced. A method for facilitating replacement of individual components for the system utilizes the pressure generating device.

Abstract: A coupling arrangement for use in coupling a patient interface to the skin of a patient includes an adhesive arrangement and an application system. The adhesive arrangement includes: a substrate material having a first surface and a second surface opposite the first surface, a first adhesive material provided on the first surface, and a second adhesive material provided on the second surface. The application system is disposed on the first adhesive material and includes a number of separate portions, with each portion formed from a film material. Each separate portion includes: a base disposed on at least a portion of the first adhesive material, and a tab coupled to an interior edge of the base and extending upward and away therefrom, the tab being sized and configured to be grasped by the patient at an end portion opposite the interior edge.

Abstract: The present application describes a system for curing moldable material. The system comprises an energy source, a mold, and/or other components. The mold comprises internal mold surfaces forming a mold cavity. The mold is formed from one or more materials configured to absorb electromagnetic radiation emitted by the energy source. The mold has a hot zone and a cold zone. The hot zone and the cold zone have the one or more materials thereof comprising at least one different physical characteristic so that the hot zone and the cold zone absorb the electromagnetic radiation at different rates and/or in different amounts. The hot zone absorbs more electromagnetic radiation than, and/or electromagnetic radiation faster than, the cold zone.

Abstract: A patient interface for use in delivering a flow of a breathing gas to an airway of a patient includes a body that defines a cavity therein that is structured to receive the flow of breathing gas. A first aperture defined in the body is positioned and structured to communicate the flow of breathing gas from the cavity to an airway of the patient. A second aperture defined in the body is sized and configured to provide a pathway between the cavity and an ambient environment in which the body is disposed. The patient interface further includes a restrictor element that is selectively coupled to the body. The restrictor element includes a blocking portion that obstructs at least a portion of the second aperture.

Abstract: A conduit for use in a pressure support system for communicating a flow of pressurized gas to the airway of a patient includes a first strip of a first material disposed helically about a central longitudinal axis such that subsequent helical convolutions of the first strip are disposed adjacent each other, and a second strip of a second material disposed helically about the central longitudinal axis along the first strip. The second strip is coupled between the subsequent helical convolutions of the first strip so as to form a hollow conduit. The first material is structured to prevent the passage of fluids therethrough. The second material is structured to allow passage of a liquid therethrough while inhibiting passage of gases therethrough.

Abstract: A retention assembly is for a patient interface device. The patient interface device includes a cushion member structured to engage a face of a patient. The retention assembly includes: a retention member structured to be coupled to the cushion member; a headgear member; a first interconnect member removably coupled to the retention member; and a second interconnect member removably coupled to the headgear member. The second interconnect member is removably coupled to the first interconnect member in order to couple the headgear member to the retention member.

Abstract: A retention assembly is for a patient interface device. The patient interface device includes a cushion member structured to engage a face of a patient. The retention assembly includes: a retention member structured to be coupled to the cushion member; a headgear member; a first interconnect member removably coupled to the retention member; and a second interconnect member removably coupled to the headgear member. The second interconnect member is removably coupled to the first interconnect member in order to couple the headgear member to the retention member.

Abstract: An angular interlock for a swivel feature formed using injection molding techniques is described herein. In one exemplary embodiment, the swivel feature is used for a conduit for delivering breathing therapy to a patient, and includes an outer swivel component and an inner swivel component formed using a two-shot molding technique. The outer swivel component is formed first out of a material, such as polycarbonate, having a low shrink rate, whereas the inner swivel component is formed of a material, such as polypropylene, having a high shrink rate. The material for the inner swivel component is injected into the formed outer swivel component and allowed to cool, creating a clearance. The outer swivel component includes an angular interlock protrusion that allows the inner swivel component to be formed without creating an interface about the angular interlock protrusion, which typically occurs with standard rectangular interlocks.

Abstract: An interconnect assembly (100, 300, 400) is for a support assembly (2) that includes a retention member (4) and a strap member (6). The interconnect assembly includes a number of female interconnect members (110, 210, 310, 410) with a first body member (112, 212, 312) and a first magnet (116, 216, 316, 416) coupled to the first body member. The first body member is connected to the retention member and has an aperture (114, 214, 314, 414). The interconnect assembly also includes a number of male interconnect members (150, 250, 350, 450) with a second body member (152, 252, 352) and a second magnet (160, 260, 360, 460) coupled to the second body member. The second body member is connected to the strap member and includes a protrusion (154, 254, 354, 452, 454) structured to be located within the aperture. When the protrusion is located within the aperture, the first magnet is attracted to the second magnet, thereby removably connecting the first body member to the second body member.

Abstract: A fluid coupling member includes a housing having an interior and an exterior, the interior of the housing defining an airflow path through the fluid coupling member, a valve member pivotally attached to the interior of the housing, and at least one protrusion formed on the valve member or the housing. The at least one protrusion is structured to prevent the valve member from becoming stuck in a downward folded position against the housing.

Abstract: A patient interface face contact element comprises a surface for contacting the face of a patient, and a connection face for coupling the patient interface face contact element to a support using a magnetic coupling. The support is also provided as well as the complete patient interface. Headgear strap clips can also be retained magnetically.

Abstract: The present system is configured to absorb, using a fluid medium in a reservoir, electromagnetic radiation to heat the fluid medium. The fluid medium may then conduct heat into a mold cavity formed by interior mold surfaces of at least two mold pieces. The fluid medium may heat up to, but not beyond, a phase transition temperature of the fluid medium, reducing instances of accidental damage to moldable material in a mold cavity during thermally-accelerated curing of the moldable material. In some instances a mold may be placed in liquid contained by the reservoir. In some instances, a mold may have integral reservoirs in individual mold pieces.

Abstract: A headgear component for a patient interface device includes a member having a first surface and a second surface opposite the first surface, the member including at least one of a textile material and a foam material, the member having a plurality of vent holes extending therethrough, and a plurality of moisture wicking members provided on the first surface, the moisture wicking members covering the vent holes and being made of a hydrophilic material.

Abstract: A patient interface device includes a frame having a central portion with a patient facing side, an opposite outward facing side, a first plurality of magnetic elements secured on or in the patient facing side, and a first aperture defined therethrough. The first aperture having a first portion extending from the outward facing side toward the patient facing side which is structured to be coupled to a delivery conduit and a patient side portion defined by a wall which extends outward from the patient facing side forming a hub. The device further includes a cushion having a patient contacting side which is structured to sealingly engage about an orifice or orifices of a patient, an opposite frame contacting side including a second aperture defined therein which is sized and configured to engage about the hub, and a second plurality of magnetic elements for magnetically coupling the cushion to the frame.

Abstract: A patient interface face contact (14) element comprises a surface for contacting the face of a patient, and a connection face for coupling the patient interface face contact element to a support (15) using a magnetic coupling (30). The support is also provided as well as the complete patient interface. Headgear strap clips can also be retained magnetically.

Abstract: A respiratory interface device is provided. The respiratory interface device includes a patient interface device, a patient circuit, and a pressure generating assembly. Pressure generating assembly includes a first pressure generating device and a second pressure generating device. Patient circuit includes a reduced conduit.

Abstract: A maintaining member is for a patient interface device. The patient interface device includes a cushion member structured to engage a face of a patient. The maintaining member has body structured to be located on a single side of the face of the patient. The body includes a coupling portion structured to be coupled to the cushion member, and a maintaining portion extending from the coupling portion, the maintaining portion having a receiving portion located opposite and facing the coupling portion, the receiving portion being concave facing in a direction toward the coupling portion in order to maintain the patient interface device on the face of the patient.