A nasal or full-face mask frame includes a main body and a vent assembly provided to the main body. The vent assembly includes a plurality of holes arranged in at least one column. The holes are positioned on a relatively flat and/or non-recessed portion of the main body.

A nasal assembly for delivering gas under positive pressure to a patient for treatment of sleep disordered breathing includes an air connector to be connected to an air supply tube for delivering a supply of gas. The air connector is to be positioned on top of the head. A nasal interface engages the patient's nose to direct the breathable gas to the patient's nose. A pair of flexible side portions support the nasal interface in a desired position on the patient's face. Each side portion has a conduit with a top portion and a bottom portion. Each conduit is arranged between the patient's eye and ear. A central portion joins the top portions of the conduits. The air connector is pivotally connected to each of the supply tube and the central portion.

A breathing mask for use in administering inhalable medications to a patient in need of an inhaled drug is provided. The mask disclosed herein is particularly useful for use with very young children. The mask is made from a flexible molded plastic silicone or elastomeric material, and has an anthropometrically/anatomically/ergonomically contoured shape to provide a good seal, a comfortable fit, and minimal dead space within the mask. The airway is aligned with nose. There may be an orifice for use with a soother device to calm a child using the mask. Also provided is a visual flow indicator to provide an indication of the quality of the seal of the mask on the face.

An interface for positive pressure therapy includes a mask assembly. The mask assembly comprises a mask seal that is adapted to underlie the nose. The mask seal extends up the lateral sides of the nose. The mask seal has a primary seal below the nose and a secondary seal alongside the nose. The mask seal comprises a rolling hinge that permits one portion of the mask seal to deform relative to another portion of the mask seal. In one configuration, the portion of the mask seal that underlies the nose is configured to deform relative to a lower portion of the mask seal.

A patient interface including a seal-forming structure with a textile membrane. The textile membrane has at least one hole such that the flow of air at a therapeutic pressure is delivered to at least an entrance to the patient's nares. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in a cavity of a plenum chamber throughout the patient's respiratory cycle, in use. The textile membrane includes a first portion that is held in a relaxed state and a second portion that is held in a taut state. The taut state of the second portion is configured to allow the seal-forming structure to include a three-dimensional shape that has multiple curvatures.

A breathing mask for use in administering inhalable medications to a patient in need of an inhaled drug is provided. The mask disclosed herein is particularly useful for use with very young children. The mask is made from a flexible molded plastic silicone or elastomeric material, and has an anthropometrically/anatomically/ergonomically contoured shape to provide a good seal, a comfortable fit, and minimal dead space within the mask. The airway is aligned with nose. There may be an orifice for use with a soother device to calm a child using the mask. Also provided is a visual flow indicator to provide an indication of the quality of the seal of the mask on the face.

A method and apparatus can be used in the selection of correctly sized respiratory interfaces. The method includes the use of light beams to project sizing markers onto a patient's face, which enables the size of the patient's facial features to be measured relative to a set of interface sizes. A sizing apparatus can include a light source and beam splitters that will refract and project the light source into a series of beams that can be aligned on a patient's face in order to measure the features of the patient.

A non-invasive ventilation system may include at least one outer tube with a proximal lateral end of the outer tube adapted to extend to a side of a nose. The at least one outer tube may also include a throat section. At least one coupler may be located at a distal section of the outer tube for impinging at least one nostril and positioning the at least one outer tube relative to the at least one nostril. At least one jet nozzle may be positioned within the outer tube at the proximal lateral end and in fluid communication with a pressurized gas supply. At least one opening in the distal section may be adapted to be in fluid communication with the nostril. At least one aperture in the at least one outer tube may be in fluid communication with ambient air. The at least one aperture may be in proximity to the at least one jet nozzle.

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.

A facial sealing segment for a respiratory device includes a sealing flap adapted to sealingly engage the face of a user. The sealing flap is disposed about, and defines, a cutout adapted to receive one or both of the mouth or nares of the user. The facial sealing segment further includes a number of selectively removable portions formed in the sealing flap about the cutout. Each removable portion is defined in the sealing flap by a tear portion. The facial sealing segment may be customized by a method that includes removing at least one of the removable portions by separating the at least one removable portion from the remainder of the sealing flap by severing along the tear portion thereof.