Abstract: A conveyor assembly for raising and feeding debris such as fallen branches from an orchard floor to a processor such as a wood-chipper is provided. The conveyor assembly comprises a body including a floor having a leading end for location adjacent ground level and a trailing end for location above the leading end in use. A ground contact arrangement is located toward the leading end extends beneath the leading end to thereby raise the leading end above ground level. A powered leading feed roller is disposed adjacent the leading end of the floor to direct members from ground on to the floor. A powered, primary infeed roller is located rearward the leading infeed roller and is arranged to move toward and away from the floor to accommodate members between said roller and the floor and urge the members, such as fallen branches rearward for entry into an inlet of the wood-chipper.

Abstract: Provided herein are compounds of Formula (I): and forms thereof, including compositions thereof and uses therewith for treating spinal muscular atrophy.

Abstract: A hair removal tool or device for removing depilatory cream from any part of the body typically where unwanted hair grows, including without limitation the face, legs, underarms, arms, intimate areas, chest and back. The device can also be used to apply or more uniformly spread the depilatory cream to make the cream more effective prior to removal. The device can also be used for applying and removing other skin treatment lotions such as an exfoliating lotion. The hair removal device includes a scraper portion having an edge for removing hair from skin as the edge moves along the skin and scrapes the depilatory cream; and a receptacle portion coupled to the scraper portion and having a receptacle for collecting the scraped depilatory cream and removed hair.

Abstract: Disclosed are systems and methods for managing consent to share data from a user device. In some examples, the system stores user identifiers referenced to the user's individual consent preferences. The consent preferences may include data types, data generating devices to which the user consents, types of third parties the user consents to share the data with and other consent preferences. Third parties may communicate with the system, and determine whether a user has consented to share their data.

Abstract: An apparatus assesses a condition of a patient. The apparatus may contain a patient interface for communicating a treatment generated by a respiratory treatment apparatus to the respiratory system of a patient. The apparatus may also include a sensing module containing one or more electrochemical sensors to sense chemicals in exhaled breath in real time, or over an extended period of time. The apparatus may also include one or more collectors to accumulate a breath condensate over an extended period of time. The sample collectors may contain an absorbent material, and may also be adapted for replacement within a sensing module. The absorbent material may also include a preservative for preserving a chemical component of the breath, such as an analyte of the exhaled breath.

Abstract: A gas delivery component of a CPAP system is configured to magnetically connect to a second gas delivery component of the CPAP system to deliver a pressurized flow of breathable gas to a patient's airways. The gas delivery component includes a lumen forming a first part of a gas flow path for the breathable gas. A connection end of the gas delivery component is configured to engage the second gas delivery component. In addition, a magnetic connection assembly is located at the connection end and includes a magnet positioned at least partially within the lumen. The magnetic connection assembly is configured to magnetically secure the gas delivery component to the second gas delivery component.

Abstract: A gas delivery component of a CPAP system is configured to magnetically connect to a second gas delivery component of the CPAP system to deliver a pressurized flow of breathable gas to a patient's airways. The gas delivery component includes a lumen forming a first part of a gas flow path for the breathable gas. A connection end of the gas delivery component is configured to engage the second gas delivery component. In addition, a magnetic connection assembly is located at the connection end and includes a magnet positioned at least partially within the lumen. The magnetic connection assembly is configured to magnetically secure the gas delivery component to the second gas delivery component.

Abstract: A patient interface assembly is configured to deliver a positively pressurized flow of breathable gas to a patient's airways. The patient interface assembly includes a patient interface configured to sealingly engage the patient's face and comprises a chamber configured to receive the pressurized flow of breathable gas. The patient interface assembly also includes headgear configured to support the patient interface on the patient's head and be tightened to one of a plurality of discrete tension settings. The headgear includes a tensioning element that is configured to contract in length to one of a plurality of discrete lengths when subjected to an electrical signal. Each discrete length of the tensioning element corresponds to a respective one of the plurality of discrete headgear tension settings.

Abstract: A patient interface assembly is configured to deliver pressurized gas to the patient's airways. The patient interface assembly includes a patient interface structure that is configured to sealingly engage the patient's face. The patient interface includes a receptacle. The patient interface assembly further includes headgear configured to support the patient interface structure on the patient's head. The headgear includes a clip that is receivable by the receptacle. The receptacle and the clip together form a multiple stage connection arrangement in which each of the multiple stages corresponds to an interlocked position of the clip in the receptacle. Each stage is associated with a corresponding range of headgear tension.

Abstract: A breathing apparatus includes components, including, but not limited to, a flow generator, a patient interface, and a delivery conduit. A connector for connecting components of the breathing apparatus includes a male connector, including a recess, extending from a first component, and a female connector, including a lever pivotally connected thereto, extending from a second component. A switch indicates a connection state of the connector. The switch includes a ring provided in an end of the first or second component and the ring includes a projection extending through an aperture in the end of the first or second component. The projection is movable between a first position and a second position to indicate the state of the connector.

Abstract: Flame resistant fabrics made from yarns of cellulose fiber, polyamide fiber, and oxidized polymeric biregional fiber are provided. The fabrics comprise about 20 to about 90 percent by weight of cellulose fiber, about 3 to about 45 percent by weight of polyamide fiber and about 5 to about 35 percent by weight of an oxidized polymeric biregional fiber comprising an oxidized polymer selected from the group consisting of acrylonitrile-based homopolymers, acrylonitrile-based copolymers, acrylonitrile-based terpolymers, and combinations thereof.

Abstract: A breathing apparatus includes components, including, but not limited to, a flow generator, a patient interface, and a delivery conduit. A connector for connecting components of the breathing apparatus includes a male connector, including a recess, extending from a first component, and a female connector, including a lever pivotally connected thereto, extending from a second component. A switch indicates a connection state of the connector. The switch includes a ring provided in an end of the first or second component and the ring includes a projection extending through an aperture in the end of the first or second component. The projection is movable between a first position and a second position to indicate the state of the connector.

Abstract: A patient interface assembly is configured to deliver pressurized gas to the patient's airways. The patient interface assembly includes a patient interface structure that is configured to sealingly engage the patient's face. The patient interface includes a receptacle. The patient interface assembly further includes headgear configured to support the patient interface structure on the patient's head. The headgear includes a clip that is receivable by the receptacle. The receptacle and the clip together form a multiple stage connection arrangement in which each of the multiple stages corresponds to an interlocked position of the clip in the receptacle.

Abstract: Headgear for a patient interface includes at least one headgear strap and an indicator provided to the at least one headgear strap structured to indicate attainment of a desired adjustment setting of the headgear in response to headgear tension applied to the at least one headgear strap.

Abstract: A patient interface for treatment of a user having a respiratory disorder includes a nasal portion having at least one nasal portion aperture adapted to be in communication with a supply of pressurized gas for delivery to at least one nasal opening of the user, and a mouth portion having at least one mouth portion aperture also adapted to be in communication with the supply of pressurized gas to deliver the pressurized gas to an oral cavity of the user's mouth. The at least one mouth portion aperture is separate from the at least one nasal portion aperture, and the patient interface is adapted to limit a flow of the pressurized gas out of the at least one aperture of the mouth portion to be no greater than a flow of the pressurized gas out of the at least one nasal portion aperture.

Abstract: A pressure impulse mitigating barrier which includes a water gel sheet having an array of protrusions formed from the water gel; and/or a layer having a plurality of disruptor particles is provided. Such a structure may protect an entity from the effects of pressure impulse, e.g. from damage caused by projectiles or from explosive blast.

Abstract: A patient interface for treatment of a user having a respiratory disorder includes a nasal portion having at least one nasal portion aperture adapted to be in communication with a supply of pressurized gas for delivery to at least one nasal opening of the user, and a mouth portion having at least one mouth portion aperture also adapted to be in communication with the supply of pressurized gas to deliver the pressurized gas to an oral cavity of the user's mouth. The at least one mouth portion aperture is separate from the at least one nasal portion aperture, and the patient interface is adapted to limit a flow of the pressurized gas out of the at least one aperture of the mouth portion to be no greater than a flow of the pressurized gas out of the at least one nasal portion aperture.

Abstract: An apparatus assesses a condition of a patient. The apparatus may contain a patient interface for communicating a treatment generated by a respiratory treatment apparatus to the respiratory system of a patient. The apparatus may also include a sensing module containing one or more electrochemical sensors to sense chemicals in exhaled breath in real time, or over an extended period of time. The apparatus may also include one or more collectors to accumulate a breath condensate over an extended period of time. The sample collectors may contain an absorbent material, and may also be adapted for replacement within a sensing module. The absorbent material may also include a preservative for preserving a chemical component of the breath, such as an analyte of the exhaled breath. The technology may provide treatment recommendations based on the detected condition of the breath condensate or the chemical components thereof.

Abstract: For the mobility impaired, it can be difficult to reach the hair and face to apply shower products such as soap, shampoo, and conditioner in a shower. Examples described herein can facilitate automatic dispensing of liquid shower products into a stream of water through a showerhead. Additionally, the flow of the liquid shower products into the stream of water can be manually controlled at a height lower than the shower head, so that a user with a limited range of motion can control the flow without needing to reach up to the height of the shower head.

Abstract: A breathing apparatus includes components, including, but not limited to, a flow generator, a patient interface, and a delivery conduit. A connector for connecting components of the breathing apparatus includes a male connector, including a recess, extending from a first component, and a female connector, including a lever pivotally connected thereto, extending from a second component. A switch indicates a connection state of the connector. The switch includes a ring provided in an end of the first or second component and the ring includes a projection extending through an aperture in the end of the first or second component. The projection is movable between a first position and a second position to indicate the state of the connector.