A patient interface includes a plenum chamber pressurisable to a therapeutic pressure, and a seal-forming structure constructed and arranged to seal with a region of a patient's face surrounding an entrance to a patients airways. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in the plenum chamber throughout a patients respiratory cycle in use. The patient interface also includes a positioning and stabilizing structure configured to hold the seal-forming structure in a therapeutically effective position on a patients head. The positioning and stabilizing structure includes a rear strap arranged to contact an occiput of the patients head. The rear strap is constructed from a first material is arranged to contact a temporal region of the patients head, and a second material arranged to contact the occiput of the patients head. The second material is silicone.

A respiratory interface, such as a mouthpiece, having a vestibular shield overlapping a user's teeth and gums, a gases passageway extending through the vestibular shield allowing for the passage of the gases through mouthpiece and an extra oral seal associated with the gases passageway, wherein the passageway in use causes gases to be diffused when exiting from the gases passageway. Mouthpiece may have an adjustment mechanism to alter distance between the vestibular shield and the extra-oral seal. The interface may include an elbow having a vent.

An oxygen concentrator (100) may have a moisture conditioning system. In some implementations, the concentrator includes a compressor to induce feed gas into the concentrator. A first pathway may receive the feed gas from the compression system. The first pathway may be configured to draw moisture to produce moisture reduced feed gas. The first pathway may lead the moisture reduced feed gas to sieve bed(s) which produce oxygen enriched air with the moisture reduced feed gas. An accumulator may be configured to receive the produced oxygen enriched air from the sieve bed(s). A second pathway from the accumulator may apply the drawn-out moisture to the produced enriched air to produce humidified enriched air. A third pathway may transfer the drawn-out moisture from the first pathway to the second pathway. An outlet coupled with the second pathway may release the humidified enriched air from the concentrator for a user.

The present disclosure provides a noise reduction device. The noise reduction device may include a noise receiving component, a noise reduction component, a processing component, and a housing. The noise receiving component may be configured to receive acoustic noise information of a scanning environment where a medical device is located. The processing component may be configured to control the noise reduction component to generate sound information matching the acoustic noise information received by the noise receiving component. The housing may be configured to support the noise receiving component and the noise reduction component.

The present invention relates to a negative pressure wound therapy device, system and method. The negative pressure wound therapy device is connected with a dressing, and comprises a housing, a control circuit board, a pump, and an aspiration conduit. The pump generates negative pressure. The pump may comprise a voltage-actuated deformation element (such as piezoelectric vibration element) to push fluid from an aspiration end to a discharge end. The aspiration conduit has a pump end and a dressing end. The pump end is fluidly connected to the aspiration end of the pump, and the dressing end is fluidly connected to the dressing used for covering a wound. The control circuit board is disposed in the housing, controls the pump to generate the negative pressure in the aspiration conduit, and applies negative pressure to the wound covered by the dressing via the aspiration conduit.

A snore blocking helmet for comfortably minimizing snore impact on others includes a helmet body having a front portion, a rear portion, a right portion, a left portion, a top portion and a bottom perimeter forming an inside. The front portion has a visor aperture and a plurality of vent apertures extending through to the inside. A visor is rotatably coupled to the helmet body to cover and alternatively uncover the visor aperture. A plurality of fans is coupled within the inside adjacent the plurality of vent apertures. A control housing is coupled through the front portion. A plurality of controls is coupled to the control housing and is in operational communication with the plurality of fans. A power source is coupled to the control housing and is in operational communication each of the plurality of controls and the plurality of fans.

A relaxation mask includes: a main body that defines a pair of eye cavities; and a light diffuser. The light diffuser includes a first lens that is disposed within a first one of the eye cavities. A first ledge is disposed along a top edge of the first lens and extends outwardly therefrom. A first light emitting component is supported on the first ledge and is configured to fire downward into the first lens.

A patient interface including a seal-forming structure having a mouth portion that forms at least part of the mouth plenum and is configured to seal around the patient's mouth and a nasal portion that is configured to seal with the patient's nares. The nasal portion includes a nasal plenum positioned to receive pressurized gas from the mouth plenum. The seal-forming structure also includes a clip configured to connect the mouth plenum to the nasal plenum and act as a conduit for the flow of the pressurized gas from the mouth plenum to the nasal plenum. The clip includes a mouth portion end configured to engage the mouth portion, a nasal portion end configured to engage the nasal portion, and a pair of wings protruding from the nasal portion end into an interior of the nasal plenum so that the wings engage an interior surface of the nasal plenum.

Methods and devices for blending of fluids are disclosed. A fluid blender has a fluid inlet to receive a fluid, a nozzle with a convergent shape tapering down towards a nozzle end, a mixing chamber with holes arranged on a wall, and a mixture outlet having a divergent shape. In some aspects, a rotary sleeve is externally placed around the wall. The rotary sleeve has slits with a variable shape along its lateral extension. In other aspects the fluid blender has inlet tubes with check valves and a blending tube. An inlet tube has an adjustable orifice to adjust flow inside the blender.

Disclosed are apparatus, systems and devices for providing modular connectivity to a respiratory therapy device. Certain forms relate to an apparatus for supplying a flow of breathable gas at positive pressure for respiratory therapy comprising a pressure generator in a housing, at least one electrical connector to connect to a connectivity module, and a cavity for receiving the connectivity module. Different forms of connectivity module may be provided. This allows for flexibility of connectivity in a respiratory device while allowing for simple installation and removal of the connectivity module.