Aspects of the subject disclosure may include, for example, receiving information about a task to be completed by a user, receiving information about the user and receiving information about a physical environment of the user. The subject disclosure may further include creating one or more immersion objects based on the information about the task, the information about the user and the information about the physical environment, creating an immersive environment including the one or more immersive objects and at least a portion of the physical environment of the user, and communicating to an extended reality (XR) device of the user information about the immersive environment to create an immersive experience for completion of the task by the user. Other embodiments are disclosed.

A steam inhaler includes a steam chamber housing having mounted therein a heater assembly. The steam chamber housing defines a steam chamber adapted to receive water. A fitting mounted to the steam chamber housing has a steam conduit section extended toward an exterior vent opening, a nozzle conduit section extended from the steam conduit, and a fresh air conduit section extended from the steam conduit section at a location downstream of the nozzle conduit section. The fitting is configured such that steam flows freely from the steam chamber, through the steam conduit section toward the exterior vent opening, a suction provided at the nozzle redirects at least a portion of the steam into the nozzle conduit section toward a mask, and the fresh air conduit directs fresh air into the steam conduit section to reduce a temperature of the steam exiting the exterior vent opening.

A personal respiratory isolation system (PRIS) provides a personal, negative pressure environment for a patient or user that reduces contamination and spread of pathogens exhaled by the patient into the environment. The PRIS includes an enclosure to receive the patient's head (such as a hood and a drape) and a negative pressure source which draws ambient air into the interior of the enclosure and draws air within the enclosure's interior (including the exhalations of the patient, including any contaminants and/or pathogens) out of the enclosure via a fluid port into a container for biohazard processing or disposal. The PRIS may allow positive air pressure therapeutic treatments to be delivered to the patient within the negative pressure environment, and the PRIS may maintain a constant pressure within the interior of the enclosure. The PRIS may include a transparent, hinged face shield for ease of patient observation and/or access.

Disclosed is an article for use with apparatus for heating smokable material to volatilize at least one component of the smokable material. The article includes a foam. The foam includes smokable material, such as tobacco. Also disclosed is a system, comprising an article and apparatus. The article includes a foam including smokable material. The apparatus is for heating the smokable material to volatilize at least one component of the smokable material. The apparatus includes a heating zone for receiving at least a portion of the article.

In one aspect, the disclosure relates to an injection device configured for expelling of a dose of a medicament. The injection device comprises a housing configured to accommodate a medicament reservoir, and a drive mechanism comprising an electric propulsion configured to mechanically interact with the medicament reservoir and configured to withdraw or to expel an amount of the medicament from the medicament reservoir. The injection device has at least a first interface directly or indirectly connected to the electric propulsion and configured to connect to a second interface of an auxiliary electronic device. The electric propulsion is controllable by the auxiliary electronic device when the first interface and the second interface are interconnected.

An oxygen concentrator may have a compressor to feed a feed gas for sieve bed(s) via a first manifold, an accumulator to receive enriched air from the bed(s) via a second manifold. It may include an outer housing for the manifolds, the compressor, and the accumulator. The housing may include an access portal to a compartment therein, for removably receiving the bed(s) as a canister assembly. The first manifold may be adjacent to the compartment and have inlet coupling(s) for removably coupling respectively with inlet(s) of the canister assembly. The inlet coupling(s) may each have a first central axis. The second manifold may be adjacent to the compartment and have outlet coupling(s) for removably coupling respectively with outlet(s) of the canister assembly. The outlet coupling(s) may each having a second central axis. The first and second central axes may form any one of an obtuse, acute, or right angle.

A charging adapter assembly for charging a vaporizer device is described herein. In some embodiments, the charging adapter may include a housing including a coupling end configured to couple to the vaporizer device. The coupling end of the housing may include a chamber having a base and at least one chamber wall defining a perimeter of the chamber. The base may include at least one charging contact. The charging adapter may include a power adapter extending from the housing. The power adapter may be configured to provide an electrical pathway between a power source and the at least one charging contact. Related systems, methods, and articles of manufacture are also described.

Modular ventilatory support systems and methods are disclosed in which a user may transition the system between a stationary configuration, an extended range configuration, and a stand-alone configuration. The modular components of the system include a compressor unit, a ventilator which may dock with the compressor unit, and a patient interface which may be connected to either the compressor unit or the ventilator unit. By rearranging these modular components into different configurations, mobility and duration of use may be optimized to fit the present needs. In the stationary configuration, mobility is most restricted, but duration of use is maximized. In the extended range configuration, mobility is enhanced, with duration of use limited by the battery power of the ventilator. In the stand-alone configuration, mobility is maximized, with duration of use limited by battery power of the ventilator and the quantity of an external gas supply.

A wearable device for providing haptic stimulations is provided. The wearable device includes: (i) a wearable structure to be worn on a portion of a user's body and (ii) an inflatable bladder, coupled to the wearable structure, that includes two or more pockets positioned at a target location on the wearable structure. Furthermore, the two or more pockets are configured to, when inflated, impart directional force(s) onto the user at the target location that impede movement of the portion of the user's body. Additionally, the directional force(s) are caused by the two or more pockets interfering with each other, when inflated. In some embodiments, (a) the portion of the user's body is a hand of the user, (b) the target location is a finger joint on the user's hand, and (c) the directional force(s) imparted onto the user at the target location impede flexion of the user's finger.

A minimally invasive circulatory support platform that utilizes an aortic stent pump or pumps. The platform uses a low profile catheter-based techniques and provides temporary and chronic circulatory support depending on the needs of the patient. Also described is a catheter-based temporary assist pump to treat patients with acute decompensated heart failure and provide circulatory support to subjects undergoing high risk percutaneous coronary intervention (“PCI”). Further described is a wirelessly powered circulatory assist pump for providing chronic circulatory support for heart failure patients. The platform and system are relatively easy to place, have higher flow rates than existing systems, and provide improvements in the patient's renal function.