Abstract: A patient interface includes a seal forming portion, a pad, and a cushion. The seal forming portion may have a base surface and a plurality of fibers fixed to and extending away from the base surface for contacting a patient's skin. The cushion may have at least along a portion of the circumference a first structure having an elongate section joined with at least one end section oriented substantially perpendicular or at an angle to the elongate section. A first end A of the elongate section may be connected or connectable to a frame member. The end section may be provided at an opposing second end B of the elongate section. The pad may have a resilient foam material layer with the seal forming portion. The pad may be adapted to be connected to the cushion.

Abstract: A patient interface includes a seal forming portion, a pad, and a cushion. The seal forming portion may have a base surface and a plurality of fibers fixed to and extending away from the base surface for contacting a patient's skin. The cushion may have at least along a portion of the circumference a first structure having an elongate section joined with at least one end section oriented substantially perpendicular or at an angle to the elongate section. A first end A of the elongate section may be connected or connectable to a frame member. The end section may be provided at an opposing second end B of the elongate section. The pad may have a resilient foam material layer with the seal forming portion. The pad may be adapted to be connected to the cushion.

Abstract: The present technology relates to a pad for forming a seal forming structure against a user's skin for use with a patient interface, the pad comprising, a base layer, a fibre layer comprising a plurality of fibers for contacting a patient's skin, and a connection layer for connecting the fibers to the base material, wherein the base layer and/or the fibre layer is/are adapted to act as a reservoir for substances. Furthermore, it relates to a set of pads, a kit and a patient interface.

Abstract: The present technology relates to a tub for a humidifier comprising a container made of a first material, a heating element, and a lining made of a second, preferably biocompatible, material different from the first material, wherein the container comprises a base and a side wall defining a reservoir for a supply of liquid to be evaporated, the heating element is provided on the base of the container, and the lining covers the heating element and a substantial portion of the inner surface of the side wall of the container.

Abstract: A connecting element produces a pipe connection between the connecting element and a plastic pipe or a metal-plastic composite pipe by using axial pressing technology. The connecting element has at least one support body provided with circumferential external ribs for press-fitting an expanded end of the pipe onto, and includes at least one circumferential collar, wherein the connecting element between the circumferential collar and the nearest circumferential external rib to the circumferential collar includes a pre-stop for limiting the sliding onto of the expanded end of the pipe. The distance between the edge of the pre-stop facing the circumferential external ribs and the edge of the circumferential collar facing the pre-stop is 0.10 times to 0.30 times the length of the support body.

Abstract: A pipe connection includes at least one end of a plastic pipe or a metal plastic composite pipe and one connecting element with at least one support body provided with circumferential ribs, onto which the end of the pipe is slid. For the expansion ratio R(exp) of the pipe connection, the following applies: 0.05<R(exp)=[D(max)/D(internal)]?1<0.35 wherein D(max) stands for the maximum external diameter of the circumferential ribs and D(internal) for the internal diameter of the pipe.

Abstract: A water reservoir for an apparatus for humidifying a flow of breathable gas includes a reservoir base including a cavity structured to hold a volume of liquid and a conductive portion provided to the base. The conductive portion is adapted to thermally engage with a heater plate to allow thermal transfer of heat from the heater plate to the volume of liquid. The conductive portion includes a thin film comprising a non-metallic material, and the thin film includes a wall thickness less than about 1 mm.

Abstract: A patient interface includes a seal forming portion, a pad, and a cushion. The seal forming portion may have a base surface and a plurality of fibers fixed to and extending away from the base surface for contacting a patient's skin. The cushion may have at least along a portion of the circumference a first structure having an elongate section joined with at least one end section oriented substantially perpendicular or at an angle to the elongate section. A first end A of the elongate section may be connected or connectable to a frame member. The end section may be provided at an opposing second end B of the elongate section. The pad may have a resilient foam material layer with the seal forming portion. The pad may be adapted to be connected to the cushion.

Abstract: It is discloses a patient interface comprising a seal forming portion, a pad, and a cushion. The seal forming portion may comprise a base surface and a plurality of fibers fixed to and extending away from said base surface for contacting a patient's skin. The cushion may comprise at least along a portion of the circumference a first structure having an elongate section joined with at least one end section oriented substantially perpendicular or at an angle to the elongate section. A first end A of the elongate section may be connected or connectable to a frame member. The end section may be provided at an opposing second end B of the elongate section. The pad may comprise a resilient foam material layer with the seal forming portion. The pad may be adapted to be connected to the cushion.

Abstract: A sliding sleeve for axially sliding onto an expanded end of an all-plastic pipe or a plastic composite pipe, into which is slid a support body having circumferential external ribs of an connecting element is made of an elastically-deformable polymeric material. The internal surface of the sliding sleeve has an average roughness value Ra in a range starting from 1 ?m to half of the average wall thickness of the sliding sleeve. In another embodiment, the inner surface of the sliding sleeve has a plurality of macroscopic irregularities, the depth of which does not exceed half of the average wall thickness of the sliding sleeve.

Abstract: The present invention relates to a tub configured to receive a volume of liquid for a humidifier, comprising at least one plastic component and at least one metal component, which together form a space for receiving said volume of liquid, wherein the at least one metal component and the at least one plastic component are attached to each other by means of a silicone seal. Furthermore, the invention relates to method for manufacturing a tub for a humidifier.

Abstract: The present specification is directed a method manufacturing a patient interface for treatment of sleep disordered breathing using air pressure by delivery of air to a patient's airway. The method includes locating a shell, a first sub section of a seal forming structure, and a first section of the seal forming structure in a tool. The first sub section includes a groove. The first section is constructed from a thermoformable material. The method further includes introducing a moudling material to the tool and overmolding the shell, the first sub section, and the first section. The moulded material forms a second sub section of the seal forming structure that connects the first sub section to the shell and fully encloses the first section within the groove.

Abstract: The present invention relates to a tub configured to receive a volume of liquid for a humidifier, comprising at least one plastic component and at least one metal component, which together form a space for receiving said volume of liquid, wherein the at least one metal component and the at least one plastic component are attached to each other by means of a silicone seal. Furthermore, the invention relates to method for manufacturing a tub for a humidifier.

Abstract: A water reservoir for an apparatus for humidifying a flow of breathable gas includes a reservoir base including a cavity structured to hold a volume of liquid and a conductive portion provided to the base. The conductive portion is adapted to thermally engage with a heater plate to allow thermal transfer of heat from the heater plate to the volume of liquid. The conductive portion includes a thin film comprising a non-metallic material, and the thin film includes a wall thickness less than about 1 mm.

Abstract: The present specification is directed to a seal forming structure for a patient interface for delivery of air to a patient's airway, wherein the seal forming structure comprises a first section of a thermoformable material and a second section of another material. The present specification is also directed to a patient interface comprising such a seal forming structure, wherein the patient interface further comprises a shell. The specification is also directed to methods for manufacturing such a patient interface.

Abstract: A water reservoir for an apparatus for humidifying a flow of breathable gas includes a reservoir base including a cavity structured to hold a volume of liquid and a conductive portion provided to the base. The conductive portion is adapted to thermally engage with a heater plate to allow thermal transfer of heat from the heater plate to the volume of liquid. The conductive portion includes a thin film comprising a non-metallic material, and the thin film includes a wall thickness less than about 1 mm.

Abstract: The present technology relates to a pad for forming a seal forming structure against a user's skin for use with a patient interface, the pad comprising, a base layer, a fibre layer comprising a plurality of fibers for contacting a patient's skin, and a connection layer for connecting the fibers to the base material, wherein the base layer and/or the fibre layer is/are adapted to act as a reservoir for substances. Furthermore, it relates to a set of pads, a kit and a patient interface.

Abstract: A sliding element for transmitting a sliding force onto a sliding sleeve which is provided to be slid, at least in sections, onto a widened end region of a tube has at least one stop surface with a recess, wherein the stop surface is designed for arranging the sliding sleeve on the stop surface and the recess is designed for the arrangement of a portion of the tube. The stop surface has an edge facing away from the recess and an edge facing the recess. The stop surface comprises at least two raised regions which are arranged spaced apart from that edge of the stop surface which faces away from the recess, and/or the stop surface comprises two extension portions which extend the stop surface on both sides of the recess beyond the end of a respective limb.

Abstract: A sliding sleeve connection between an expanded end of an all-plastic pipe or of a plastic composite pipe and a connecting element includes an expanded end of an all-plastic pipe or of a plastic composite pipe; a connecting element having at least one support body provided with circumferential external ribs, onto which the expanded end of the all-plastic pipe or of the plastic composite pipe is slid, and at least one circumferential collar; and a sliding sleeve made of elastically deformable polymer material axially slid onto the expanded end. The connecting element includes a pre-stop between the circumferential collar and the nearest circumferential external rib to the latter. The pre-stop constitutes a limitation for sliding onto the end of the pipe. The end of the sliding sleeve facing the circumferential collar protrudes beyond the end of the pre-stop facing the circumferential external rib.

Abstract: The invention relates to a patient ventilation or breathing device and components therefore for use in all forms of respiratory apparatus ventilation systems including invasive and non-invasive ventilation, positive airway pressure therapy, Continuous Positive Airway Pressure (CPAP), and particularly Bi-Level therapy and treatment for sleep disordered breathing (SDB) conditions such as Obstructive Sleep Apnea (OSA), and for various other respiratory disorders and diseases. The invention particularly relates to a blower, to a blade, to a gasket, to a cable, to an impeller, to a gas inlet and inlet member, to an improved air path or fluid flow path and components thereof, and/or to a modular ventilation or breathing device as referred to above and particularly incorporating one or more of the other aspects of the invention.