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 for delivering a flow of air to an entrance of a patient's airways includes a plenum chamber configured to receive a flow of air, one or more prongs configured to deliver the flow of air from the plenum chamber to the entrance of a patient's airways, a rigid frame configured to engage a cheek of the patient in use, and a headgear coupled to the rigid frame and configured to engage with the patient's head to locate the one or more prongs in use. The rigid frame includes a central portion that overlaps and extends past the plenum chamber in an anterior direction and in a posterior direction. In addition, the rigid frame is disengaged from the plenum chamber in the anterior direction.

Abstract: An apparatus for generating a decoded two-channel signal, comprising: a parametric decoder for providing parametric data for a second set of second spectral portions and a two-channel identification identifying for a second spectral portion of the second set of second spectral portions either a first two-channel representation for the second spectral portion of the second set of second spectral portions or a second two-channel representation for the second spectral portion of the second set of second spectral portions, the second two-channel representation being different from the first two-channel representation; and a frequency regenerator for regenerating the second spectral portion of the second set of second spectral portions depending on a first spectral portion of a first set of first spectral portions, the parametric data for the second spectral portion of the second set of second spectral portions and the two-channel identification for the second spectral portion of the second set of second spectral

Abstract: A patient interface comprises a frame, a headgear, a manifold and two nasal prongs. The frame may be recessed from the face of the patient, and preferably from the manifold so that the manifold may deform or move with respect to the face of the patient. The manifold may be further configured to be compliant in the direction of engagement with the patient's face, such as in the anterior direction. These features may allow the manifold to engage with the face of the patient, such as the upper lip, without exerting a significant pressure which may lead to patient discomfort. The manifold may also be configured to be rotatable with respect to the frame, for example by a grip feature which may be configured to be held in one hand for rotation.

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 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: Systems and methods are provided for performing, at a server, a stack trace of an application at a predetermined interval to generate a plurality of stack traces, where each stack trace of the plurality of stack traces is from a different point in time based on the predetermined interval. The stack trace is performed when the application is operating normally and when the application has had a failure. The plurality of stack traces stored are indexed by timestamp. The server may determine a state of the application based on at least one of the plurality of stack traces. The server may condense data for at least one of the plurality of stack traces that are indexed using predetermined failure scenarios for the application. The server may generate a report based on the condensed data and the state of the application, and may transmit the report for display.

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: Embodiments of the present invention include a method of processing time series metrics (TSM) data. The method includes receiving a TSM data point for a metric, the TSM data point indicating an identifier (ID) of the metric, getting a persistence policy associated with the metric, selecting a first resolution database according to the persistence policy, storing the TSM data point in the first resolution database, selecting a second resolution database according to the persistence policy; and when the second resolution database is defined, storing the TSM data point in a staging file for the second resolution database.

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: A rotary table for a coordinate measuring apparatus for receiving and mounting a workpiece to be measured is provided. The rotary table has a rotatable main rotary table body and a clamping chuck, which is arranged on the rotatable main rotary table body and which has a clamping chuck receptacle for receiving the workpiece to be measured, the rotary table also having at least one master, which is arranged outside the clamping chuck receptacle, and/or at least one fastener for a master, which is provided in addition to the clamping chuck receptacle. In addition, a coordinate measuring apparatus with a corresponding rotary table is provided.

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: Disclosed is a particularly lightweight breathing mask for respiratory applications or as personal protective equipment, in which the rigid component is produced from thermoplastic films by means of high-pressure forming. The base material of the rigid component is available in a flat form and can thus be printed or coated in a variety of ways before processing; this allows properties to be introduced into the mask that would not be feasible in a conventional injection molding process. The use of film instead of injection-molded components enables a significant reduction in weight and thus an improvement in wearing comfort for the user.

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.