Abstract: An electrically heated smoking system includes a shell and a replaceable mouthpiece. The shell includes an electric power supply and electric circuitry. The mouthpiece includes a liquid storage portion and a capillary wick having a first end and a second end. The first end of the wick extends into the liquid storage portion for contact with liquid therein. The mouthpiece also includes a heating element for heating the second end of the capillary wick, an air outlet, and an aerosol forming chamber between the second end of the capillary wick and the air outlet. When the shell and mouthpiece are engaged or connected, the heating element is in electrical connection with the power supply via the circuitry, and a flowpath for air is defined from at least one air inlet to the air outlet via the aerosol forming chamber. In use, liquid is transferred from the liquid storage portion towards the heating element by capillary action in the wick.

Abstract: The invention relates to a positioning sputum suction laryngeal mask. The positioning sputum suction laryngeal mask comprises a mask body and a mask body tube, wherein the mask body comprises a mask body bottom plate and a mask main body arranged on the mask body bottom plate, a central region in the mask main body is provided with a mask body cavity communicated with the mask body tube, a stomach decompression tube corresponding to the stomach mouth is arranged on the back side of the mask body bottom plate, and the stomach decompression tube is isolated from the mask body cavity through the mask body bottom plate. The positioning sputum suction laryngeal mask also comprises a connection suction mechanism capable of realizing negative pressure suction in a gas supply process.

Abstract: A shroud for a mask system includes a retaining portion structured to retain a frame, a pair of upper headgear connectors each including an elongated arm and a slot at the free end of the arm adapted to receive a headgear strap, and a pair of lower headgear connectors each adapted to attach to a headgear strap. The retaining portion, the upper headgear connectors, and the lower headgear connectors are integrally formed as a one piece structure.

Abstract: An apparatus for vaporizing a concentrate and/or a non-concentrate material is provided. The apparatus can include a housing, a reservoir, a vessel, and a heating element. The reservoir can be coupled to a lid of the apparatus and configured to hold the concentrate. The vessel can be disposed at least partially inside of the housing and can be configured to receive the reservoir when the lid of the apparatus is in a closed position with respect to the housing. The heating element can be configured to generate heat for heating the vessel, thereby vaporizing the concentrate in the reservoir to form an aerosol. Coupling the reservoir to the lid of the apparatus can enable the apparatus to be used for vaporizing the concentrate while decoupling the reservoir from the lid of the apparatus can enable the apparatus to be used for vaporizing the non-concentrate material. Related methods are also provided.

Abstract: A method for veterinary administration of medication to an animal, particularly a horse, is disclosed. The method involves inserting a capsule containing the medication, which is a liquid formulation, into a device connected to a tubular chamber. An atomizer is activated to atomize the medication, producing atomized medication. Before administration, a force is applied to a mask placed over the animal's muzzle, connected to the chamber. The atomized medication is then delivered to the animal. The liquid formulation, in some instances, comprises cells, cellular byproducts, or cell-derived products such as stem cells or products from human mesenchymal stem cells. This formulation may lack preservatives and may encompass peptides, proteins, growth factors, cytokines, exosomes, and extracellular vesicles. The delivery mechanism may involve deflating an air bladder to convey the atomized medication.

Abstract: Lung conditions are diagnosed and optionally treated using a functional assessment catheter or a functional lung assessment and treatment catheter. A flow restrictive component is initially placed in a bronchus or lung passageway upstream from a diseased lung region. The isolated lung region is then functionally assessed through the catheter, while the flow restrictive component remains in place. If the patient is a good candidate for treatment by occlusive or restrictive treatment techniques, the flow resistive component may be left in place. If the patient is not suitable for such treatment, the flow resistive component may be removed.

Abstract: Embodiments of the present invention disclose an equipment carrying system configured for sliding over a valveless end of a gas cylinder. The assembly includes a main body having a plurality of straps forming a webbing; a seat portion formed within the main body, the seat portion being configured to receive the valveless end of the gas cylinder; an auxiliary cylinder assembly coupled to the main body, the auxiliary cylinder assembly configured to hold a second gas cylinder; a handle coupled to the seat portion, the handle used to lift and carrying the main body; and wherein the main body, the auxiliary cylinder assembly, and the handle hang from the seat portion on the valveless end of the gas cylinder.

Abstract: The invention pertains to a capsule system for use with a medical device designed to administer atomized medication to patients. The system features a chamber containing the medication and an atomizer at a lower end for efficient drug delivery. Notably, the system incorporates a fluid sensor and electrical contacts to ensure proper operation and medication delivery. The capsule's design includes a housing with an asymmetrical transverse cross-sectional shape for unique fitting, and a tapered wall to direct medication towards the atomizer. The capsule may also connect to an external container or include a stopper for refilling medication. A specific embodiment features two chambers with a rupturing element to facilitate medication transfer. Another embodiment includes a removable container, like a vial, within the first chamber. This novel system provides improvements in accuracy, versatility, and user-friendliness, overcoming limitations in prior art.

Abstract: A medical instrument with an aerosol outlet, which is fluidically connected—via an aerosol line—to a generation device. The generation device is adapted to generate aerosol for dispensing by means of the medical instrument. In addition, a generation device is stated, which, in embodiments of the generation device, for example can be used in a device with the instrument according to the invention. The generation device comprises a mixing unit for mixing a liquid and a gas together, which mixing unit is connected to a liquid container for supplying the mixing unit with a liquid, in which case the generation device is adapted to utilize the gas pressure of a gas under pressure subjecting the liquid to a pressure in order to press the liquid out of the liquid container to the mixing unit.

Abstract: Sensing airflow and delivering therapeutic gas to a patient. At least some of the example embodiments are methods including: titrating a patient with therapeutic gas during a period of time when a flow state of breathing orifices is in a first state, the titrating results in a prescription titration volume; and then delivering the prescription titration volume of therapeutic gas to the patient when the flow state of the breathing orifices is in a second state different than the first state, the delivering only to the breathing orifices open to flow.

Abstract: The invention relates to a breathing device (1), comprising a mouthpiece (2) forming a breathing channel to form a connection between a first (3) end and a second (4) end of the mouthpiece (2). The first (3) end is configured for a user breathing into the mouthpiece through a breathing opening (5). An at least partly flexible rebreathing air chamber (6) is arranged in fluid communication with the second (4) end of the mouthpiece, thereby being in fluid connection with the breathing channel through the second end of the mouthpiece (2). The rebreathing air chamber is formed by at least partly flexible wall section(s). A wall member (7) is arranged at the second (4) end of the mouthpiece and/or attached to the rebreathing air chamber (6). The wall member (7) comprises one or more through-going openings (8) provided in the wall member (7) and/or in the breathing channel, allowing fluid communication between the rebreathing air chamber (6) and the surrounding atmosphere.

Abstract: A system for delivering a pressurized flow of breathable gas to a patient includes a patient interface and a flow generator mounted on the patient interface. The patient interface is configured to contact the patient's head and includes a frame and a cushion supported by the frame and configured to sealingly connect the patient interface to the patient's face and form a chamber between the frame and the patient's face. An inlet port in the frame is configured to receive the pressurized flow of breathable gas. The flow generator is configured to generate the pressurized flow and is capable of creating a pressure of about 2-40 cm H2O in the chamber. In addition, a pressure sensor assembly spans from an outlet port of the flow generator to the inlet port of the patient interface.

Abstract: A respirator mask for automatically activating an air-saver switch within a regulator by rotation of the regular as the regulator is mounted and dismounted from a facepiece of the mask. The mask includes a facepiece including a regulator engagement region having an aperture and a protrusion proximate the aperture, and a regulator including a regulator body having a facepiece engagement region mateably engageable with the regulator engagement region, a fluid flow path within the regulator body, and a latch within the regulator body, the latch causing obstruction of the fluid flow path when actuated. The latch is engageable with the protrusion, the regulator being rotatable within the facepiece aperture between a first rotational position and a second rotational position, rotation of the regulator within the facepiece aperture from the second to the first rotational position engaging and actuating the latch to obstruct the fluid flow path.

Abstract: A heat and moisture exchanger (IO) for tracheostomized or laryn-gectomized patients, having a valve plate and a housing, wherein: the valve plate has a radially surrounding lip, and the housing comprises a valve seat which encloses a distal opening of the housing, the valve seat has a groove for receiving the lip, the valve plate is associated with the distal opening of the housing, and the valve plate can be moved into a closed position in which the lip engages in the groove.

Abstract: A wearable face covering may include a mask including a filter and a cap, wherein the cap is configured to prevent any gas passing through the filter in a first direction from exiting the mask in the first direction; and a face shield including a partially-transparent screen, wherein the face shield is pivotally coupled to the mask.

Abstract: A system for administering at least one medication to a patient is disclosed. The system includes a resilient air bladder in fluid communication with a tubular chamber of a base unit, a capsule in fluid communication with the tubular chamber configured for carrying the at least one medication, and an atomizer disposed at least proximate to the capsule and in fluid communication with the tubular chamber. An air inlet and a first one-way valve is in fluid communication with the resilient air bladder configured to allow fresh air to enter the resilient air bladder. An air outlet and a second one-way value is in fluid communication the resilient air bladder and the tubular chamber. Fresh air and the medication atomized by the atomizer mix together within the tubular chamber.

Abstract: A method is disclosed for administering medication to conscious or unconscious patients using a device with a tubular chamber. The method involves the use of a device with a tubular chamber, wherein a liquid medication is contained within a capsule. The medication is atomized by activating an atomizer, thereby generating an atomized medication consisting of particles with a maximum diameter of four microns. The atomized medication is then dispensed into the tubular chamber. Using the device, the atomized medication is administered to the patient. In cases of unconsciousness, a resilient air bladder connected to the chamber is partially deflated, allowing air transfer into the chamber. This facilitates the administration of the atomized medication. This method enables effective medication delivery in various emergency scenarios, ensuring appropriate treatment even for unresponsive patients by providing a method of using a device with modular components.

Abstract: This disclosure describes systems and methods for providing adaptive base flow scheduling during ventilation of a patient to optimize patient-machine synchrony and accuracy of estimated exhaled as well as inhaled tidal volumes. Further, this disclosure describes systems and methods for providing adaptive inspiratory trigger threshold scheduling during the adaptive base flow scheduling. Further still, this disclosure describes systems and methods for determining an estimated leak flow and adjusting the adaptive base flow scheduling and the adaptive inspiratory trigger threshold scheduling based on the estimated leak flow. Moreover, this disclosure describes systems and methods for determining a change in the estimated leak flow and adjusting the adaptive base flow scheduling and the adaptive inspiratory trigger threshold scheduling based on the change in the estimated leak flow.

Abstract: A shroud for a mask system includes a retaining portion structured to retain a frame, a pair of upper headgear connectors each including an elongated arm and a slot at the free end of the arm adapted to receive a headgear strap, and a pair of lower headgear connectors each adapted to attach to a headgear strap. The retaining portion, the upper headgear connectors, and the lower headgear connectors are integrally formed as a one piece structure.

Abstract: A non-ventilator ET tube cap used to oxygenate a patient during an intubation procedure. The ET tube cap generally comprises an oxygen source connector configured to connect to an oxygen source via an oxygen tube. This provides oxygen to a patient via an ET tube while being intubated. The ET tube cap further includes an ET tube receiving aperture that is specifically arranged to engage an ET tube in a removable relationship prior to the ET tube connected to a ventilator while the ET tube is deployed in a patient. Optionally, the ET tube cap can comprise a pressure relief valve that opens when pressure inside of the ET tube cap exceeds a predetermined pressure threshold to prevent harm to the patient that is being intubated.