A method of manufacturing a patient interface for sealed delivery of a flow of air at a continuously positive pressure with respect to ambient air pressure to an entrance to the patient's airways includes collecting anthropometric data of a patient's face. Anticipated considerations are identified from the collected anthropometric data during use of the patient interface. The collected anthropometric data is processed to provide a transformed data set based on the anticipated considerations, the transformed data set corresponding to at least one customised patient interface component. At least one patient interface component is modeled based on the transformed data set.

A patient interface including a seal-forming structure with a textile membrane that has at least one hole such that the flow of air at a therapeutic pressure is delivered to at least an entrance to the patients nares and/or an entrance to the patients mouth. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in a cavity of a plenum chamber throughout the patients 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 respiratory assembly is provided. The assembly includes a base engaged with at least one connector and in fluid communication with a hose or fluid source for allowing the gaseous flowthrough between the at least one connector, the base and the hose or fluid source. The assembly further includes a pair of sockets engaged with the at least one connector, and a pair of posts, each post selectively engageable with at least one of the pair of sockets. Each post includes a flange that defines an opening therethrough, the openings in fluid communication with each corresponding socket of the pair of sockets. Each post further includes an adhesive adhered to each flange and configured for sealably engaging a patient's nare.

A patient interface for respiratory therapy includes a nasal interface having nasal prongs configured to contact nares of the user and form a seal. The patient interface also includes a securement portion having a pair of facial pads, each of the facial pads configured to engage the face of a user on opposing sides of the nasal interface. The facial pads are coupled to the bridging portions configured to urge the nasal interface toward the user's face to create or maintain sealing engagement between the nasal interface and the user's face. In some configurations, the securement portion and the nasal interface are detachably coupled to each other.

A passive oxygen mask and vacuum regulation system disposed in fluid communication with a vacuum scavenging array includes a passive oxygen mask dimensioned to fit over a patient's nose and mouth and having a gas inlet port and an expired gas outlet port. A vacuum regulation assembly has a vacuum regulator which includes an expired gas discharge tube disposed in fluid communication between the passive oxygen mask and the vacuum regulation assembly, and a vacuum suction tube disposed in fluid communication between the vacuum regulation assembly and the vacuum scavenging array. The vacuum regulation assembly further comprising a vacuum attenuation port through a portion of a regulator housing, wherein the vacuum attenuation port is at least partially defined by an attenuation port diameter dimensioned to reduce a vacuum suction pressure in the expired gas discharge tube to a predetermined vacuum suction pressure.

A headgear assembly includes a strap of a first flexible material with an elongate edge, and a second flexible material folded around and running along the elongate edge. The second flexible material may be an elastic material. The second flexible material may also cover an intersection or joint in the first flexible material such that the first flexible material may be made from two flexible materials layered together or joined end to end.

A sanitary device for securing a breathing tube to a patient during anesthesia administration, which also prevents leaking anesthetic gases from entering the operating room environment. The novel design allows rapid application by the user and prevents potential transmission of infectious agents to the patient while securing the breathing tube. A unique, integrated suction system efficiently evacuates leaking anesthetic gases. The device may be manufactured inexpensively and is provided in sanitary packaging. It is intended for single use.

A method of introducing a vapor of at least one substance into an inhalation flow path of a respiratory organ is provided. The method describes providing a carrier conformable to a surface of skin; providing the carrier with at least one substance; providing a barrier coupled to a surface of the carrier, the barrier being substantially impermeable to the substances carried by the carrier; providing a polyethylene coated material disposed within or atop the barrier and configured as a clamp for a septum of a user, wherein the polyethylene coated material is heat sealed within the barrier; and engaging the carrier to the surface of skin proximate an inhalation flow path of a respiratory organ with the barrier adapted to be interposed between the carrier and the skin to prevent the one or more substances from contacting the skin; wherein the substance is volatile and/or non-volatile; wherein the carrier is impregnated with nanocapsules during production. A vehicle for introducing a vapor is also provided.

A patient interface comprises a plenum chamber and a seal-forming structure. The seal-forming structure comprises a support structure arranged to support a sealing portion that is adapted to sealing engage the patient's face in use. The seal-forming structure may also include a seal biasing portion configured to inflate under pressurization within the cavity in the cushion assembly in use to extend the reach of the sealing portion and decouple the sealing portion from external forces.

A system for aligning a patient interface for use in delivering a flow of a breathing gas to the airway of a patient with an adhesive arrangement that is structured to secure the patient interface to the patient. The system includes a base that is structured to be disposed on a surface, the base having a central member protruding upward from the base to a contoured surface. The central member includes a pair of protruding alignment elements that extend further upward from the contoured surface and which are sized and structured to engage apertures in both of the adhesive arrangement and the patient interface in a manner which aligns such components with each other.