An air delivery system for providing a supply of air from a source of air at positive pressure to an interfacing structure located at the entrance to the airways of a patient includes a manifold adapted to connect with the supply of positive air pressure and at least one tube connected to the manifold and adapted to deliver the supply of air to the interfacing structure. Each tube is structured to allow movement between an open phase in which the tube allows the passage of air and a collapsed phase in which the tube is collapsed. Each tube is structured such that weight of a typical patient's head against bedding apparel is sufficient to collapse the tube from the open phase to the collapsed phase.

It is an object of the invention to increase the predictability of the MRI exam for the patients. This object is achieved by a method for classifying sound of a magnetic resonance imaging sequence into a sound category, wherein the magnetic resonance sequence comprises a one or more sound blocks, wherein individual sound blocks have signal characteristics and wherein sound blocks having similar characteristics are to be classified into the same sound category, the method comprising the steps of: receiving information about one or more gradient waveforms to be used in the magnetic resonance imaging sequence and; using a classification algorithm to map the waveform information to a sound category and; allocating a visual to the sound category.

The shell is intended to receive an injection system comprising a syringe received in a safety device which has: a body receiving the syringe; a shield movable relative to the body, for covering a needle; finger flanges extending outwardly. The shell comprises a tubular housing receiving a distal portion of the safety device and a casing receiving the finger flange, and further comprising: several snap features which flex outwardly during insertion of the finger flange in the casing, the finger flange being inserted distally from a distal face of the snap feature in the mounted position; and a protrusion located distally from each distal face, which exerts an inward biasing force on the finger flange in the mounted position.

A personal therapy system includes a sensory stimulation pack having a heating device and/or a scent-emitting device, and a holder including a holder body receiving the sensory stimulation pack within a cavity. The holder body has two disc-shaped body pieces releasably attachable to contain the sensory stimulation pack, and vents for outputting heat or scent from the cavity. Surfaces of the holder body have selectively smooth or not smooth textures for varied tactile stimulation of a user.

A positive exhalation pressure device (1) is described. The device (1) comprises a housing (2) having an annular chamber (5), a chamber inlet (6) configured to permit air into the chamber, a chamber outlet (7) configured to permit air out of the chamber, and a mouthpiece (8) in fluid communication with the chamber inlet. A movable body such as a ball (3) is disposed in the housing within the annular chamber and configured to revolve around the annular chamber in response to flow of air through the chamber from the chamber inlet to the chamber outlet. The movable body is configured to at least partially block the chamber outlet as it revolves around the annular chamber causing cyclical fluctuations in airflow resistance.

Provided is a Dry Powder Inhaler (DPI) arrangement comprising a DPI arranged in fluid communication with a spacer device (110) comprising a bag (112) and a body (118) including inlet (114) and opposed outlet (116), the inlet (114) and opposed outlet (116) being provided on, and integral with, the body (118). The body (118) and bag (112) combine to form chamber (120) for operatively receiving vaporised dry powder medication. The inlet (114) and outlet (116) each are in the form of a port that is in fluid flow communication with the chamber (120). The inlet (114) and outlet (116) define, and are separated by, a broad V-formation formed as part of the body (118). The body (118) further includes an elliptical lower perimeter (118.1) defining flange (118.2), for demountably receiving bag (112)

Provided is a spacer device (110) for delivery of drugs via a nebuliser device, the space device (110) comprising a bag (112) and a body (118) including inlet (114) and opposed outlet (116), the inlet (114) and opposed outlet (116) being provided on, and integral with, the body (118). The body (118) and bag (112) combine to form chamber (120) for receiving aerosolised medication. The inlet (114) and outlet (116) each are in the form of a port that is in fluid flow communication with the chamber (120). The inlet (114) and outlet (116) define, and are separated by, a broad V-formation formed as part of the body (118). The body (118) further includes an elliptical lower perimeter (118.1) defining flange (118.2), for demountably receiving bag (112).

Embodiments of a method (e.g., for operating a robotic device such as a dog device, etc.) can include: receiving one or more inputs (e.g., sensor input data, etc.) at a dog device (e.g., at one or more sensors of the dog device; a robotic dog device; etc.) from one or more users and/or other suitable entities (e.g., additional dog devices; etc.); determining one or more events (and/or a lack of one or more events), such as based on the one or more inputs (and/or a lack of one or more inputs); processing (e.g., determining, implementing, etc.) one or more scenes based on the one or more events (and/or lack of one or more events); and/or performing one or more output actions with the dog device, based on the one or more scenes (e.g., individual scenes; scene flows; etc.).

An air delivery system for providing a supply of air from a source of air at positive pressure to an interfacing structure located at the entrance to the airways of a patient includes a manifold adapted to connect with the supply of positive air pressure and at least one tube connected to the manifold and adapted to deliver the supply of air to the interfacing structure. Each tube is structured to allow movement between an open phase in which the tube allows the passage of air and a collapsed phase in which the tube is collapsed. Each tube is structured such that weight of a typical patient's head against bedding apparel is sufficient to collapse the tube from the open phase to the collapsed phase.

A device for directing a nebulized mixture includes a receiver, disposed at lower end of the device, to receive a nebulizer, an exhaust port to expel a nebulized mixture from the device, and a passage to transport the nebulized mixture from the nebulizer to the exhaust port. The device has an external shape of a novelty.