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 process for ventilating a patient as well as a device—patient module (20)—operating according to the process, wherein, for example, a body weight value concerning an estimated body weight of the patient is transmitted to a patient module (20) intended for ventilating the patient, wherein the patient module (20) automatically selects ventilation parameters (52) fitting the body weight value on the basis of the body weight value and wherein the ventilation of the patient is carried out with the selected ventilation parameters (52).

Abstract: An inhaler article includes a body extending along a longitudinal axis from a mouthpiece end to a distal end with an endpiece element at the distal end. A capsule cavity is defined within the body and extends along the longitudinal axis a cavity length. The capsule cavity includes a helical feature on or in an inner surface of the capsule cavity. The helical feature extends along the cavity length. An air inlet region is between the endpiece element and the capsule cavity. The air inlet region has an air inlet and an air passageway extending from the air inlet to the capsule cavity. A porous element defines a downstream end of the capsule cavity. A mouthpiece air channel extends from the capsule cavity, through the porous element to the mouthpiece end.

Abstract: In some embodiments, the present disclosure provides a method to process high pressure air into low pressure breathing air for one or more sealing and locking helmets and/or one or more air respirators. Other embodiments include a system configured to perform such a method and a manufacturing process of making such a system. In some embodiments, the breathing system automatically fills a local reserve bottle by pressure equalization. In this regard, the secondary supply bottles will fill the backup bottle when the console module operator (CMO) connects the secondary air supply to the system. The backup bottle will then be isolated from depletion during normal operation by means of a check valve to prevent back flow of the emergency cylinder into the secondary air supply. The local reserve bottle will protect against loss of air on any of the high pressure air hoses.

Abstract: A respiratory treatment device comprising at least one chamber, a chamber inlet configured to receive air into the at least one chamber, at least one chamber outlet configured to permit air to exit the at least one chamber, and a flow path defined between the chamber inlet and the at least one chamber outlet. A restrictor member positioned in the flow path is moveable between a closed position, where a flow of air along the flow path is restricted, and an open position, where the flow of air along the flow path is less restricted. A vane in fluid communication with the flow path is operatively connected to the restrictor member and is configured to reciprocate between a first position and a second position in response to the flow of air along the flow path.

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: The present disclosure relates to a breathing assistance apparatus for providing a breathing assistance to a user. The breathing assistance apparatus includes a first/second source configured with a first/second buffer. The first/second fluid is controllably transferred from the first/second source to the first/second buffer using any or combination of a first/second pressure regulators and one or more first/second valves. A mixing chamber configured with the first buffer and the second buffer to receive and mix the first fluid and the second fluid. A delivery tank configured with the mixing tank to controllably receive the third fluid through one or more fourth valves and a third pressure regulator. A user feed mask having an inlet configured with the delivery tank and user's face facilitating breathing assistance to the user.

Abstract: A patient interface structure includes a cushion configured to sealingly engage the patient's face and a front that is more rigid than the cushion. The cushion includes a forward opening, a rearward opening that is opposite the forward opening and a continuous sealing surface. The continuous sealing surface has a mouth sealing portion configured to seal around the patient's mouth and a nasal sealing portion configured to seal around both of the patient's nasal airways. The front plate includes an air inlet configured to both receive the pressurized respiratory gas and secure headgear to the patient interface structure. In addition, the nasal sealing portion includes at least one aperture that is separate from the rearward opening. Also, the front plate, the mouth sealing portion and the nasal sealing portion together form a common chamber.

Abstract: A patient interface for delivery of a supply of pressurised air or breathable gas to an entrance of a patient's airways comprising: a cushion member that includes a retaining structure and a seal-forming structure permanently connected to the retaining structure; a frame member attachable to the retaining structure; and a positioning and stabilising structure attachable to the frame member.

Abstract: A mask apparatus includes a mask body and a mask body cover coupled to the mask body. The mask body includes a front surface, a rear surface, and a pair of air ducts disposed at left and right sides of the front surface. The mask body is configured to mount a pair of fan modules at suction sides of the pair of air ducts. The mask body cover covers the pair of air ducts and the pair of fan modules. The mask body defines a cover coupling groove along an edge of the mask body, and the cover coupling groove is coupled to an edge of the mask body cover.

Abstract: The present disclosure relates generally to medical devices and, more particularly, to a gas mixing system for a medical ventilator. A gas mixer is provided to adjust the oxygen concentration of environmental air for a blower-based ventilator, by adjusting the mix of air upstream of the ventilator and providing the mixed air to the ventilator's environmental air inlet.

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 patient interface of a respiratory therapy system is provided, and includes: a. a mask body; b. a mask seal secured to the mask body and configured to form a seal with the user's face, at least around the user's mouth; the mask body and mask seal being arranged to define an interior breathing Chamber of the patient interface; and c. an inlet to the breathing chamber configured to receive a flow of breathable gases into the breathing chamber. To assist in allowing a user to speak clearly whilst wearing/using the patient interface, a user actuatable speech valve is provided on the patient interface and is operable to selectively occlude and open a speech flow path from the breathing chamber to atmosphere when the user wishes to speak.

Abstract: A medical ventilation monitoring system is provided. The system includes: a patient ventilation unit defining an airflow path, and arranged so that when the unit is applied to a patient, the airflow path is in fluid communication with the patient's airway. The patient ventilation unit includes: an airflow sensor positioned to sense the presence of ventilation airflow to or from the patient and a communication link. The system also includes at least one processor arranged to communicate with the ventilation unit by the communication link. The at least one processor is configured to: provide an initial treatment protocol for providing care to the patient, receive data regarding a current condition of the patient from the ventilation unit, and determine an updated treatment protocol. The updated treatment protocol includes applying ventilation at an updated ventilation volume or at an updated ventilation rate based on information from the airflow sensor.

Abstract: Methods and systems for increasing oxygen concentration. An example system includes an oxygen valve configured to be coupled to an oxygen source, an oxygen plenum coupled to the valve, and a mixing valve. The mixing valve includes an oxygen inlet coupled to the oxygen plenum, an ambient-air inlet, and an outlet configured to be attached to an inlet of a blower of a ventilator. The system also includes a pressure sensor, coupled to the oxygen plenum, and a control device communicatively coupled to the pressure sensor and the oxygen valve. The control device receives a differential pressure, measured by the pressure sensor, and based on the measured differential pressure, generates a control signal to control the oxygen valve to maintain a target pressure of gas within the oxygen plenum.

Abstract: An oscillating positive expiratory pressure apparatus having a housing defining a chamber, a chamber inlet, a chamber outlet, a deformable restrictor member positioned in an exhalation flow path between the chamber inlet and the chamber outlet, and an oscillation member disposed within the chamber. The deformable restrictor member and the oscillation member are moveable between an engaged position, where the oscillation member is in contact with the deformable restrictor member and an disengaged position, where the oscillation member is not in contact with the deformable restrictor member. The deformable restrictor member and the oscillation member move from the engaged position to the disengaged position in response to a first exhalation pressure at the chamber inlet, and move from the disengaged position to an engaged position in response to a second exhalation pressure at the chamber inlet.

Abstract: An adjustable heat and moisture exchanger (HME) for use with a breathing apparatus to humidify air comprising: an inlet for coupling to a source of air, and an outlet for delivering air to a patient and an air flow path between them, HME material in the flow path with two or more surfaces exposed to the air flow path to exchange humidity between patient air flow and an inlet air flow, at least one adjuster for adjusting the configuration of the HME material and/or the air flow to alter the air flow over the surfaces of the HME material to alter the exchange of humidity.

Abstract: A respiratory training device providing both inspiratory and expiratory functional evaluation and training, as well as independent regulation of both the inspiratory and expiratory airway resistance levels used during training. The respiratory training device also includes data acquisition, recording, storage, retrieval and display functions for airway pressure monitoring data to provide functional evaluation, physiological monitoring, and diagnostic features. The respiratory training device allows the user to easily develop and follow precise and advanced training protocols, and utilize the respiratory device in both the clinical and home setting.

Abstract: A fastening unit, in particular a fastening unit for modules which are intended to supply a user of a breathing mask or breathing hood with breathable air, and to such modules. The fastening unit is designed to secure one module relative to another module, and has a first component part for assembly with the other module and a second component part for assembly with the module. The second component part is rotatable, by means of the first component part, about a predetermined angle relative to the first component part; and first and second subcomponents within the region of the defined angle can engage with each other in a plurality of positions.

Abstract: An exercise with oxygen therapy (EWOT) apparatus for rejuvenating oxygen-depleted cell tissue and simulating high altitude oxygen conditions. The EWOT apparatus includes a first cylindrical bladder for providing oxygen-enriched air and a second bladder for providing lower-purity hypoxic air. The first bladder is retained within an open, lightweight rectangular-shaped frame having vertical frame members. An air supply source provides the oxygen-enriched and hypoxic air to the first and second bladders, respectively. A control switch, which can be manually and/or programmed to automatically operate, selectively delivers the oxygen-enriched and/or hypoxic air to a breathing mask worn by a user while exercising on exercise equipment. The first bladder includes a plurality of weights which provide a positive pressure to the air therein.

Abstract: A positive airway pressure device includes a primary housing and a humidification system. The primary housing includes an outer edge, a first electronic connection portion, and a blower configured to deliver a vapor to a patient. The humidification system includes a water reservoir configured to hold a liquid, a heating plate in thermal communication with the water reservoir, a second electronic connection portion, and a lid configured to selectively shield the second electronic connection portion. The primary housing is configurable between at least two positions relative to the humidification system. The at least two positions include a first position in which the lid at least partially shields the second electronic connection portion and a second position in which the outer edge of the primary housing forces open the lid such that the first electronic connection portion mates with the second electronic connection portion.

Abstract: A patient interface may include a plenum chamber and a positioning and stabilising structure. The plenum chamber may include a seal-forming structure and a fascia portion. At least a medial portion of the fascia portion is flexible. In embodiments, the patient interface may include a rigidiser to control flexing of the fascia portion.

Abstract: A respiratory assistance apparatus includes a conduit connecting a flow generator and an outlet. The conduit includes a venture formation. The apparatus further includes an oxygen inlet in fluid communication or selective fluid communication with an oxygen outlet. The oxygen outlet is directed into the conduit and toward a mouth of the venture formation. The flow generator provides a flow path for air to enter the conduit when the flow generator is not operating.

Abstract: A pulse modulated oxygen dispensing and pressurization system provides a variable range of controlled oxygen bolus to an enclosed breathing environment supporting and maintaining required pressure conditions in accordance with desired flow demand. As oxygen is consumed by the user from within the enclosed breathing environment, the exhaled gases and moisture are conditioned or vented to acceptable levels by additional systems associated with the environment. These additional systems cause an ongoing need to replenish the oxygen within the environment and maintain the required partial pressure of oxygen. Specific to one of a plurality of modes of operation, the system responds to changes in regulated output pressure by delivering a precisely metered periodic bolus volume of oxygen to support a requirement of the environment volume. The bolus is variable based on a plurality of factors to increase and decrease changes in rates of flow required to maintain regulated pressure.

Abstract: A mask system for delivery of respiratory therapy to a patient includes a nares portion and a mouth portion and an inlet conduit connected to at least one of the nares portion and the mouth portion to deliver the pressurized, breathable gas. The mask system is adapted to selectively utilize the nares portion and/or the mouth portion in a first mode utilizing both the nares portion and the mouth portion, and in a second mode utilizing the nares portion and not utilizing the mouth portion.

Abstract: Systems and devices for monitoring, detecting, and removing fluid build-up found at various regions along a tracheal tube of an intubated patient. The fluid management system includes pressure and flow sensors for detecting whether there is fluid at the various regions along the tracheal tube, and a means for drawing out the fluid into collection jars. The system also includes lavage features that is able to rinse different the various regions along a tracheal tube. Also disclosed are respiration insertion devices that either couple to existing tracheal tubes or incorporate tracheal tubing, where the respiration insertion body has channels and ports that contact various regions along the tracheal tube. The combination of the fluid management system and the respiration insertion devices effectively monitor and remove fluid at various locations along a tracheal tube of an intubated patient.

Abstract: An improved safety device for a self-contained breathing apparatus, and an improved self-contained breathing apparatus having thermal imaging capabilities.

Abstract: A nebulizer device aerosolizes (or vaporizes) liquid drawn from a liquid reservoir via a fluid flow path into a nebulization chamber. An inlet port is coupled to an external air supply and leads through a check valve and Venturi nozzle (e.g. a duckbill valve) into the chamber to direct an air stream across an opening of the fluid flow path. A discharge port leads from the chamber to a user mask, mouthpiece or canula, where the aerosol or vapor mixture can be inhaled. A filtered outlet port isolates exhaled material from the external environment. Multiple discrete heating elements may be placed around the fluid flow path to preheat the liquid. If the liquid is sufficiently volatile, heating may vaporize the material which can condense back into an aerosol after mixing with the air stream. A set of check valves direct one-way fluid flow and prevent leakage or spillage of material from the device.

Abstract: A respiratory therapy apparatus is operable to deliver multiple types of therapy to a patient. The apparatus includes a main housing and a nebulizer tray that selectively attaches to a bottom of the main housing. The apparatus also includes a filter housing unit having an antenna surrounding a pneumatic passage and a transponder chip coupled to the antenna. The main housing has also has an antenna that surrounds a respective pneumatic passage of a main outlet port of the apparatus. The main housing includes a reader that controls communication between the antennae. The main housing of the apparatus also has a pivotable hose support plate, a firmware upgrade port underneath part of the top wall of the housing, and a graphical user interface (GUI) that displays various user inputs for control of the apparatus and that displays various alert conditions that are detected.

Abstract: A gas valve is adapted for controlling the flow of a medical gas for oxygen therapy in case of spontaneous breathing. The gas valve comprises a connection component for connecting the gas valve to an external supply; and a regulating system configured for selecting and supplying a pulsating flow of medical gas or a continuous flow of medical gas, in which the regulating system comprises a first sub-regulating system for supplying a pulsating flow and a second sub-regulating system for supplying a continuous flow.

Abstract: An apparatus for use in humidifying a flow of treatment gas for a user includes: a housing; an inlet structured to receive the flow of treatment gas from a gas flow generator; an outlet structured to convey the flow of treatment gas to a patient interface device; a compartment defined in the housing, the compartment being structured to hold a volume of water therein; a primary valve disposed between the inlet and the compartment, the primary valve being structured to permit passage of the flow of treatment gas from the inlet to the compartment and to prevent passage of a fluid from the compartment to the inlet; and a secondary valve disposed between the compartment and the inlet which is structured to permit passage of a fluid from the compartment to the inlet and to prevent passage of the flow of treatment gas from the inlet to the compartment.

Abstract: An exhalation valve arrangement includes an upstream breathing gas duct, which extends along a first duct path, a downstream breathing gas duct, which extends along a second duct path, and a valve assembly having a valve body and a valve seat, which valve assembly is provided such that, in the event of a predetermined first breathing gas overpressure in the upstream breathing gas duct relative to the downstream breathing gas duct. The valve assembly permits an exhalatory breathing gas flow from the upstream breathing gas duct to the downstream breathing gas duct and, in the event of a predetermined second breathing gas overpressure in the downstream breathing gas duct relative to the upstream breathing gas duct, the valve assembly blocks a gas flow from the downstream breathing gas duct to the upstream breathing gas duct.

Abstract: A first-stage diving regulator including the profiled body, swivel turret and the cylinder connector, whereas the axis of rotation of the swivel turret is perpendicular to the body axis, thus enabling by preferable arrangement of low pressure LP ports and high pressure HP ports of the body, and preferable arrangement of low pressure LP ports in the swivel turret and proper hose configuration at any possible equipment configuration by using the same first-stage regulator.

Abstract: One aspect of the disclosure includes a respiratory valve apparatus. The respiratory valve apparatus may include: a housing having an inner chamber, an endotracheal tube connection port, a ventilator connection port, and a resuscitation bag connection port; and a piston assembly positioned within the inner chamber and including a piston having a first passageway and a second passageway through the piston, wherein the first passageway provides a first flow pathway between the endotracheal tube connection port and the ventilator or connection port when the piston is in a first position, and wherein the second passageway provides a second flow pathway between the endotracheal tube connection port and the resuscitation bag connection port when in a second position.

Abstract: A system for detecting manual ventilation and selectively delivering a high flow of oxygen. The system comprises a source of compressed oxygen coupled to a first lumen of a nasal cannula, with an oxygen flow control valve coupled to a processor to control the flow of oxygen to the nasal cannula. A second lumen of the nasal cannula is in connection with a pressure sensor and the pressure sensor in connection with the processor. The processor may receive the pressure values and be programmed to determine when manual ventilation has occurred, and send a signal to the oxygen flow control valve to send a high flow of oxygen in response to manual ventilation.

Abstract: A respiration device (1) supports cardio-pulmonary resuscitation (CPR) and a method for operating a respiration device (1) supports cardio-pulmonary resuscitation (CPR). The respiration device (1) has a control and regulation unit (7) in order to actuate an expiratory metering unit (3), and an inspiratory metering unit (2) such that, in a first phase, a current value of pressure is increased relative to a first pre-defined value (16) and such that, in a second phase, the current value of the pressure is reduced relative to the first pre-defined value (16).

Abstract: A connector that is in a fuel supply system capable of supplying a high-pressure fuel, and may reduce pulsation in a low-pressure pipe with a simple structure and extend the life of a mold is provided. A valve of the connector includes a valve seat contact surface and a tapering through hole. The valve seat contact surface axially separates from an annular valve seat and forms a forward-direction flow path due to pressure of the low-pressure fuel when the high-pressure fuel does not flow in reverse, and may come into contact with the annular valve seat when the high-pressure fuel flows in reverse. The tapering through hole is formed farther radially inward than the valve seat contact surface, forms an orifice flow path having a smaller cross-sectional area than the forward-direction flow path, and allows a reverse flow of the high-pressure fuel when the high-pressure fuel flows in reverse.

Abstract: A second stage diving regulator with separated stages that allows changing a position of connection of a LP hose for low pressure supplied from a first stage of the regulator, characterized in that around connected bodies there is a rotating ring with a valve seat and a valve terminated with a thread to which a low pressure LP coming from the first stage of the machine is connected horizontally. The rotation of the rotary ring is ensured at least in the range of 180 degrees from the starting position, through all the intermediate angles downwards towards the cylinder, up to a horizontal position opposite to the starting position, the side of the body.

Abstract: Systems and methods for effecting bariatric procedures are disclosed. Each system includes an instrument, a control valve and, optionally, a suction controller. The instrument is in the form of an elongated, flexible member having a distal end portion arranged for anchoring the instrument in the patient's stomach and for enabling fluids to be removed from the patient's stomach. Suction is applied to the patient's stomach by the distal end portion of the instrument to drain gastric fluids and to bring adjacent portions of the patient's stomach into engagement with the instrument to provide a visually perceptible delineation line along which a portion of the stomach may be resected, sealed and tested.

Abstract: A pressure regulator assembly for an SCBA includes a valve assembly having a piston, a cylinder for receiving the piston, a sealing member for engagement by the piston, a conduit extending through the piston and facilitating fluid communication between an inlet chamber and a cavity of the cylinder, and a driving assembly for facilitating the engagement and disengagement of the piston responsive to a change of pressure in the outlet chamber. A bypass assembly for an SCBA is also disclosed.

Abstract: A nasal assembly for delivering breathable gas to a patient includes a frame having lateral connector, a cushion with a pair of nozzles, and a clip to secure the cushion to the frame. The frame includes a vent channel and a plurality of vent holes. The frame/cushion includes structure (lugs/cut outs) to prevent the assembly of an unvented frame with an unvented cushion, for safety purposes. The frame includes cored portions that interface with corner lugs provided on the cushion. A patient interface includes a frame, a cushion (nasal mask, nasal-oro mask, nozzles, etc.) and a vent assembly including a pattern of vent holes including at least two rows.

Abstract: 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.

Abstract: A method for performing a medical procedure requiring effective, reliable and foolproof delivery of controlled amounts of a medical grade gas to a patient includes providing a compressed gas cylinder having a weight with medical grade gas sealed therein of at least twelve grams and not greater than fifty grams. The method also includes connecting the compressed gas cylinder to an integrated compressed gas unit including a regulator valve assembly positioned between an outlet port and an inlet port, wherein the regulator valve assembly includes a press button actuator and regulator adjustment dial. A flow control system is secured to the compressed gas unit and the medical grade gas is delivered in precisely controlled amounts by actuating the compressed gas unit and operating the flow control system to deliver the medical grade gas to vasculature of the patient.

Abstract: A valve module (20) for a ventilation system (100), includes a tube interface (21) for connection to a counter-tube interface (14) of an exhalation end (13) of a ventilation tube element (11) as well as a device interface (22) for connection to a counter-device interface (114) of an exhalation port (113) of a ventilator (110). The device interface has an exhalation valve section (24) providing an exhalation flow (93) of exhaled air (92) with an exhalation pressure (94). The exhaled air from the tube interface (21) flows through a module space (23). A ventilation tube device (10), the ventilator (110) as well as the ventilation system are provided with the valve module. Processes are provided for severing and establishing a connection between the device interface, the ventilation tube device and the counter-device interface of the exhalation port of the ventilator of the ventilation system.

Abstract: An electronic cigarette includes a housing, wherein the housing is elongate and has a head end disposed toward the user and a tail end extending away from the user. The housing comprises a bottom cover and a shell section. A battery is retained within the housing. An atomizer tank cartridge fits to the housing. An electrical heating apparatus powered by the battery. A groove is formed between the bottom cover and the shell section. A trim piece is mounted between the bottom cover and shell section. The trim piece is a hot-melt material, and connected to the groove via a heating process. The trim piece passes around an external periphery of the housing. The trim piece is an epoxy resin material. The housing further comprises a removable mouthpiece cover attached at a head end.

Abstract: The present invention relates to a respiratory therapy device (1) for the targeted assistance of a secretion removal from the airways of a patient and a method for operating such a respiratory therapy device (1). The respiratory therapy device (1) comprises a flow unit (2) for generating a respiratory airflow for an insufflation and a respiratory airflow for an exsufflation, which comprises a patient interface (3) for connecting the patient and a respiratory air interface and two fans (5, 6) fluidically connected in parallel each having an intake side (15, 16) and a delivery side (25, 26). A first fan (5) is fluidically coupled with its intake side (15) and a second fan (6) is fluidically coupled with its delivery side (26) to a switchable valve unit (7).

Abstract: A lung isolation tube assembly including a control valve that is adapted to be moved between a left lumen position, a right lumen position, and a both lumens position, a connector that is in fluid communication with the control valve, and a tube that is in fluid communication with the connector. The tube includes a left lumen that is in fluid communication with the connector and a right lumen that is in fluid communication with the connector. The assembly also includes a first cuff that is disposed around a portion of the right lumen and the left lumen and a second cuff that is disposed around the left lumen. The assembly is adapted to convey airflow or oxygen to a human lung via at least one of the left lumen and the right lumen. A method for isolating a human lung.

Abstract: The present invention relates to a tracheal coupling comprising a patient port 33, an outlet port 36, an inlet port 31 between the patient port and the outlet port, such that flow 34 from the inlet port can go to the patient port or direct to the outlet port, and a flow restriction e.g. 32 between the inlet port and the outlet port, or at the outlet port.

Abstract: A rechargeable therapeutic system for treating conditions of a user's nasal cavities, sinuses or ear canals includes a therapeutic device having a housing that includes an inlet that allows air to enter the therapeutic device. An acoustic vibrator located within the housing provides an acoustic vibration to the user, and a power supply located within the housing provides power to the acoustic vibrator. A mask is connected to the housing and configured to be applied around the nose of the user. A valve of the mask is configured to allow the user to breathe through the inlet. The mask further includes a diaphragm and a nasal cavity in which the user's nose is located when the mask is applied around the nose of the user. A recharging station is configured to provide a charging current to the power supply.

Abstract: A portable gas delivery system 10 may generally comprise a gas container 20, a regulator 30, an adapter 40 to couple the regulator 30 to the container 20, and a tube or cannula 50 and/or a mask 60 fluidly connected to the container 20. Methods of making and using the portable gas delivery system are also described.