Abstract: A face mask is provided. The face mask includes a body portion that is configured to be placed over a mouth and at least part of a nose of a user such that the air of respiration is drawn through the body portion. The body portion includes a baffle layer which helps prevent penetration from a fluid striking the mask. The baffle layer has an outer and an inner surface with a plurality of projections extending from one of the outer or inner surfaces. The baffle layer aids in absorbing energy associated with fluid striking the body portion of the mask. The baffle layer distributes fluid away form the point of impact in the channels between the projections.

Abstract: Containers for incrementally dispensing pressurized contents are described. The containers comprise a vessel suited to contain pressurized contents, a port integral with the vessel and through which pressurized contents contained in the vessel can be released from the vessel, preferably incrementally in approximately equal amounts, and a measuring device disposed in or otherwise associated with the vessel such that the quantity or amount of contents in the vessel can be measured or assessed. The measuring device senses ambient conditions in the vessel and, directly or with other components, indicates, for example, the amount of pressurized contents remaining in the vessel and displaying it to an observer. Devices for incrementally dispensing pressurized contents from such containers are also described.

Abstract: An inhaler and a direct current power supply voltage control device with a relatively simple structure that output a predetermined drive voltage according to a specified time interval to a drive object such as a heating resistor. An inhaler 1 is equipped with a liquid ejection head 9, and is set so that a user is able to inhale liquid droplets ejected from the liquid ejection head 9. The inhaler 1 includes: specifying means 4, 5 and 6 for specifying a drive voltage 701 based on preset voltage data 501 respectively corresponding to preset time intervals that respectively specify the drive voltage 701 of the liquid ejection head 9 in synchronization with the start of control of a drive signal 302 of the liquid ejection head 9; and drive means 3 and 7 for driving the liquid ejection head 9 according to the drive signal 302 at the specified drive voltage 701.

Abstract: A system for supporting a breathing passage of a patient may include a cannula and an insertion apparatus. The cannula may be configured to be at least partially inserted into a breathing passage of a patient for supporting the breathing passage during sleep. The cannula may include an insertion end configured to be inserted through a nasal passageway portion of the breathing passage. The insertion apparatus may include a nasal applicator operable to guide the cannula through the nasal applicator and into the nasal passageway, and a support frame coupled to the nasal applicator and configured to be releasably coupled to the patient to position the nasal applicator proximate to the nasal passageway.

Abstract: A method and a CPAP apparatus for characterizing mask systems provided. The CPAP apparatus can be calibrated by including sensors configured to measure flow and pressure. When the flow generator is fitted to a new or changed mask system, a method for calibrating the flow generator for the new or changed mask system. The method includes determining air flow characteristics using flow measurements made during a first test period when the flow through the mask system is open, measuring or estimating pressure in the mask system during a second test period when the flow through the mask system is blocked and determining air flow characteristics of the diffuser of the mask system using the air flow characteristics of the air delivery hose determined during the first test period and the pressure measurements made during the second test period.

Abstract: A medication dispenser includes a thermal drop generator ejector head. Medication is maintained in a pressurized container connected to a valve under the control of control electronics and to a compliant chamber. Fluid flows from the container to the chamber and to the ejector head. In a first mode the dispenser is operable to dispense aerosolized medication. In a second mode the ejector head is purged with fluid from the container to maintain the ejector head.

Abstract: In order to improve the security and reliability of administration of powdered pharmaceuticals through dry powder inhalers, the invention proposes an inhaler (1) for powdered medicaments, comprising an activating device (4) for manual engagement by the patient for repeatedly metering a dose of medicament to be administered to the patient, and further comprising an advancing mechanism (25) for advancing a counter or indexing means (8) each time the activating device (4) has been engaged by the patient so that a dose of medicament has been released for administration to the patient, wherein the counter or indexing means (8) comprises an index (9), the index (9) being detectable by a detection means (10) of the inhaler, and the detection means (10) being coupled to a locking mechanism (12), the locking mechanism (12) blocking the activating device (4) and/or any transportation mechanism (5) of the inhaler (1) delayed by a predetermined number of metering cycles since detection of the index (9), and a cartridge (

Abstract: A respiratory mask assembly for delivering breathable gas to a patient includes a frame and a headgear assembly removably attachable to the frame. The headgear assembly includes a pair of side portions and a rear portion that interconnects the pair of side portions. The pair of side portions includes at least one strap. The rear portion has at least one strap constructed of at least two layers of material. One of the layers of material has a more rigid construction than the other of the layers of material to resist compression of the at least one strap of the rear portion in a first direction which resists movement of the at least one strap of the pair of side straps in the first direction.

Abstract: A mask system is provided to fit pre-adult patients, or patients having facial features that are very small or child-like, e.g., patients having dimensions in the lower 5%-10% of the population. For example, the headgear and/or cushion are dimensioned to accommodate this range of patients.

Abstract: A conduit for a breathing circuit includes a heater associated, at least in part, with a hydrophilic layer. The purpose of the heater is to evaporate any condensed liquid collecting in the conduit, which is first sucked up by the hydrophilic layer. The heated wick reduces the risk of collected water being passed to the patient and causing choking fits or discomfit. It is preferred that the heated wick lies freely in the conduit to settle at low points in the conduit where condensation may collect.

Abstract: A sound dampening apparatus to be disposed in pneumatic connection with a respiratory support system. The respiratory support system may comprise a source of medical gas, a plurality of pneumatic connections and a patient interface. The sound dampening apparatus comprises an inlet, an outlet, and an outer case which forms a sound dampening chamber. As the medical gas flows through the sound dampening apparatus, the noise energy associated with the flow of medical gas is reduced.

Abstract: A pressure demand regulator assembly for use with a breathing apparatus having a valve assembly that includes an inlet for connection to a source of breathing gas, an outlet for connection to a facepiece to provide breathing gas to the user and an actuator for controlling the flow of breathing gas between the inlet and the outlet in response to the user's respiration. The regulator assembly further includes a flexible elastomeric diaphragm in operative connection with the actuator. The diaphragm is exposed to ambient pressure on a first side thereof and exposed to a positive pressure within the facepiece on a second side thereof.

Abstract: A portable hyperbaric chamber system includes a soft-sided, foldable hyperbaric chamber and a substantially rigid, removable, external support structure. The chamber generally includes a wall of a substantially non-breathable, soft-sided, and foldable material and an accessway sealable with a non-breathable closure so as to maintain a hyperbaric pressure within the chamber. The chamber also includes at least one fastener, such as a bolt or threaded stud, extending from the wall that permits the chamber to be removably attached to the support structure, thereby to maintain the chamber in an uncollapsed state when the chamber interior is not maintained at a hyperbaric pressure. The support structure includes structures complementary to the fasteners (e.g., apertures to pass bolts and locking knobs to secure bolts).

Abstract: A nebulizer and cartridge structure thereof for use in a nebulization apparatus comprises a first cartridge accommodation space and a second cartridge accommodation space. The first cartridge accommodation space includes at least one connection bottom, and the second cartridge accommodation space includes at least one connection side. Moreover, the second cartridge accommodation space is disposed under a lower connection position of the first cartridge accommodation space. The connection bottom is connected to the connection side to form an included angle that can be a lead angle. The lead angle further includes a fillet angle or a chamfering angle. Accordingly, the nebulizer and the cartridge structure can efficiently reduce the residues of liquid medicament.

Abstract: An oxygen concentrator comprises an oxygen reservoir and adsorbent columns that each have an inlet, an outlet, and a bed of adsorbent material. The concentrator also comprises an air inlet, an exhaust outlet, and a vacuum pump for pumping nitrogen rich gas from one of the column inlets to the exhaust outlet. A product control pump pumps oxygen rich gas from one of the column outlets to the oxygen reservoir. A control valve controls flow in and out of the columns by selectively connecting the air inlet to one column inlet, connecting the vacuum pump to another column inlet, and connecting the product control pump to a column outlet. A motor drives the vacuum pump and control valve to produce vacuum swing adsorption (VSA) cycles in which oxygen-rich product gas is separated and accumulated in the reservoir.

Abstract: Method and arrangement for adjusting nitrogen and oxygen concentrations within regions of an aircraft. The method includes separating nitrogen from ambient air onboard an aircraft thereby establishing a high-concentration nitrogen supply and then dispensing high-concentration nitrogen from the supply to a fire-susceptible, non-habitable region of the aircraft where the high-concentration nitrogen is reservoired thereby decreasing the capability for the atmosphere therein to support combustion. Oxygen is also separated from the ambient air thereby establishing a high-concentration oxygen supply that is dispensed to an occupant cabin of the aircraft thereby increasing the level of oxygen concentration within the cabin to a level greater than the naturally occurring concentration of oxygen at the experienced internal cabin pressure.

Abstract: An underwater breathing device, such as a snorkel, may include an exhalation valve. The exhalation valve is configured to produce positive end-expiratory pressure in the airway of a user of the underwater breathing device in order to reduce the overall work of underwater breathing. The exhalation valve includes a plate defining an exhalation port. The exhalation valve also includes a flexible membrane that is sealable against a surface of the plate and is sized and positioned to be capable of sealing the exhalation port. The flexible membrane is configured to have a sealed position in which the flexible membrane seals the exhalation port such that substantially no exhaled air escapes the snorkel. The flexible membrane is also configured to have an unsealed position in which exhaled air escapes the snorkel.

Abstract: An underwater breathing device, such as a snorkel, may include an exhalation valve. The exhalation valve is configured to produce positive end-expiratory pressure in the airway of a user of the underwater breathing device. The exhalation valve includes a plate defining an exhalation port and at least one chamber port, an exhalation conduit connected to the exhalation port, and a flexible membrane that is sealable against a surface of the plate. A lower portion of the exhalation conduit is divided by a septum which divides the exhalation conduit and the exhalation port into a first exhalation port connected to a first exhalation conduit and a second exhalation port connected to a second exhalation conduit. The flexible membrane is sized and positioned to be capable of sealing the first exhalation port and the second exhalation port.

Abstract: An inhaler includes an accurate and consistent mechanical dose metering system that dispenses dry powdered medicament in discrete amounts or doses for patient inhalation, a pressure relief system that manages pressure within a medicament reservoir of the inhaler to ensure consistently dispensed doses, and a dose counting system indicating the number of doses dispensed by or remaining in the inhaler.

Abstract: The present invention is a breathing improvement monitor that continuously measures involuntary breathing. The monitor is a sensor apparatus that is attached to a patient's mask which is connected to the monitoring apparatus. The sensor may be reusable and attachable and detachable to a mask or it may be an integral part of a breathing mask. The sensor technology may be any type sufficient in the art, including but not limited to solid state sensors, transducers, electromagnetic microturbines and the like. Since the mask does not have to be removed and the sensor provides constant signal to the monitoring apparatus, a real time status of a patient's involuntary breathing capability may be determined for a doctor's consideration.