Abstract: An inhalation-synchronized fluid dispenser device having a body, a reservoir containing a fluid and a propellant gas that slides axially in the body, a metering valve, a blocking element movable and/or deformable between a non-actuation position and an actuation position, and an inhalation-controlled trigger system that moves and/or deforms the blocking element from the non-actuation position towards the actuation position. The device includes an actuator fastened on the reservoir and having a proximal wall fastened on the end of the reservoir, a body that slides axially past the proximal wall, and a spring arranged between the proximal wall and a distal wall of the body, the body sliding axially past the proximal wall between a rest position and a cocked position in which the spring is compressed, such that on actuation of the trigger system, the compressed spring moves the reservoir so as to actuate the metering valve.

Abstract: An inhaler housing (14) for an inhaler (10) for inhaling inhalable substances, the inhaler having: a body (14) and a dose counter (24) with a return spring (28), wherein a distinct guide surface (162) is provided for guiding the end of the return spring into a recess (152), the distinct guide surface being wider than an entrance mouth (160) of the recess, a dose counter chamber (22) being provided which is separated from a tubular interior space (182) of the inhaler by a barrier (180), the barrier including a stepped upper wall area (184) including at least three steps (186, 188, 190, 192) at different levels, the inhaler having a valve stem block (62) having an inner bore and a valve stem block having a seal (224) in the inner bore with a second diameter which is smaller than a first diameter of the inner bore, the inhaler having a canister (150) being adapted to move during operation between 1 and 4 mm, a drive being arranged to apply a firing force of between 15N and 60N of force to the canister at a posit

Abstract: A medication delivery system including a holding chamber having an input and an output end, a backpiece coupled to the input end of the holding chamber and having an electrical circuit and an opening. An MDI incudes an insert portion moveable between an engaged position wherein the insert portion is received in the opening and a disengaged position wherein the insert portion is removed from the opening, and at least one contact that completes the electrical circuit when the insert portion is in the engaged position.

Abstract: There is described a method for operating an inhalation chamber. A duct in the inhalation chamber extends from an opening for a source of gas to an opening for patient output, the duct comprising two portions, of which the shapes are complementary to form the duct, and displaceable in relation with each other. A MDI (or pMDI) and/or a nebulizer are connected to the inhalation chamber. A relative displacement is made between the two portions of the duct to close the duct and shunt the dead volume of the inhalation chamber, making a direct passage from the source of gas to the patient. If the nebulizer or the MDI is connected, a relative displacement is made between the two portions of the duct to open the duct to an inner volume of the inhalation chamber where the nebulizer or the MDI is dispensing aerosol. Other configurations are possible.

Abstract: A wearable device for comprehensive bio-monitoring of physiologic metrics to determine metabolic, pulmonary and cardiac function and oxygen saturation measurements from breathing mask apparatuses. The device non-invasively monitors the physiologic profile of the subject, and is capable of detecting physiologic changes, predicting onset of symptoms, and alerting the wearer or another person or system. In some embodiments, the device comprises both a wearable sensor suite and a portable gas composition and flow analysis system. In preferred embodiments, it comprises a miniaturized non-invasive sensor suite for detecting physiologic changes to detect dangerous breathing or other health conditions. The acquired physiologic profile is used to generate alarms or warnings based on detectable physiological changes, to adjust gas delivery to the subject, alter mission profiles, or to transfer control of the craft or other duties away from a debilitated subject.

Abstract: A discharge head for the nasal application of pharmaceutical liquid from a pressure reservoir which has an outlet valve with a valve connector, to which force can be applied counter to a spring force in order to open the outlet valve. The discharge head has a nasal applicator which extends outward from an actuating surface and at the end of which a discharge opening is provided. The discharge opening is connected in a fluid-communicating manner to a hollow tube through an applicator channel of the nasal applicator, for connection to the pressure reservoir. The nasal applicator has an inner component connected integrally to the actuating surface and an outer component separate from the inner component and attached to the inner component in a surrounding manner. The discharge opening is provided in the outer component, and the outer component and the inner component together bound the applicator channel.

Abstract: A gas monitoring system for artificial ventilation includes: a sensor that is configured to produce a signal corresponding to a concentration of a predetermined gas in a portion which is in a respiratory circuit of an artificial ventilator, and through which both an inspiratory gas and an expiratory gas pass; a displaying apparatus that is communicable with the sensor; a processor; and a memory that is configured to store a command which is readable by the processor. When, during high-frequency oscillatory ventilation performed by the artificial ventilator, the command is executed by the processor, the processor is to configured to calculate a measurement value of the concentration based on the signal, and is configured to display at least one of a waveform corresponding to the signal and the measurement value on the displaying apparatus.

Abstract: A filler device includes a distal housing comprising a distal inner port and a distal outer port; a proximal housing comprising a proximal inner port and a proximal outer port, the proximal housing being sealingly affixed to the distal housing to form an inspiratory pathway between the distal inner port and the proximal inner port and to form an expiratory pathway between the distal outer port and the proximal outer port that is fluidly sealed from the inspiratory pathway, the inspiratory pathway being laterally adjacent the expiratory pathway; and a first filter in the inspiratory pathway or in the expiratory pathway to filter gases flowing through the inspiratory pathway or the expiratory pathway.

Abstract: Methods and systems are described herein for fluid handling and dispensing liquid substances using vaporization or nebulization in a controlled, safe manner. A dispensing device may be configured to receive one or more cartridges storing different types of vaporizable or nebulizable substances. A controller may be provided to regulate the amount of a given substance dispensed over a defined time period. Optionally, in response to detecting tampering of the dispensing device and/or a liquid cartridge the dispensing device may be disabled and/or a liquid stored in a substance cartridge may be rendered inert.

Abstract: The present invention relates to a floatable breathing device. The floatable breathing device provides includes a head unit, a snorkel, a plurality of receiving passageways, and an internal pathway. The head unit has buoyant properties and includes an ornamental shaped outer housing and an inner housing positioned within the outer housing, the inner housing forms a head receiving section, the head receiving section is provided between outer surfaces of the outer housing and is configured to be contoured to a human head. The snorkel connects to and extends from the head unit. The plurality of receiving passageways are disposed about the outer housing and receiving the snorkel, the snorkel extending through and exiting a portion of the head unit above a predetermined waterline extending along a periphery of a lower portion of the head unit thereof and identifies buoyancy of the head unit in water.

Abstract: A blower assembly including a motor, an impeller and a volute that is configured such that an inlet chamber of the volute and an outlet chamber of the volute are divided from one another by an airtight membrane and the membrane is configured to allow the transmission of pressure waves between the inlet and outlet chambers.

Abstract: A flavored attachment can adhere to the mouthpiece of an inhaler or the like, wherein the attachment is designed so that it lasts for a sufficient duration to ensure the person taking the medicine has taken the proper dosage.

Abstract: An improved spacer connects at one end to metered-dose inhalers with a connector configured to accept the mouth of the inhaler. Additionally, the spacer has a mouthpiece at its opposite end and a collapsible body made of a nonrigid material that maintains it shape with a resilient frame. The mouthpiece and body compress and nest within a cavity of the connector when the spacer is not in use. The spacer can further include a cover, a case, a vent to improve airflow, and/or a valve to cover the spacer to a valved holding chamber.

Abstract: Some embodiments provide a breathing assistance apparatus comprising a conduit for conveying gases therein, the conduit comprising circuitry. The circuitry may comprise at least one heater wire part to heat gases in the conduit, in use, and at least one sensor wire part comprising at least one sensor for monitoring a parameter of the gases in the conduit. There is also provided a controller to control provision of AC power or AC voltage to the heater wire part; and control selective reading of the sensor. The controller may be configured to read the sensor at or about a particular portion of the AC power waveform provided to the heater wire part.

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

Abstract: An apparatus for the supply of humidified gases to a patient is disclosed that comprises a gases supply passage downstream of a humidified gases supply, and upstream of a patient in use, where at least one sensor is embedded in or located on the outside of the wall of the passage. In preferred forms the wall of the passage divides the sensor(s) from a flow of gases in the passage. In use, a controller receives an output of the sensor(s) and derives from the output of the sensor(s) an estimation of a property of gases flowing through the passage or provides a control output to the humidified gases supply according to the output of the sensor(s).

Abstract: A sensing module for monitoring dosage delivery of a vaporized material, and a portable vaporization unit including the sensing module, include a light sensor that detects disruptions in a light path across a vapor channel, the disruptions caused by the vaporized material flowing through the vapor channel. The light sensor includes a UV light source, which may emit 370 nm wavelength light, and a UV light detector that converts intensity of incident light in the light path into a signal. A microprocessor of the sensing module compares the signal to a baseline measurement to determine the concentration of a medicament in the vapor; then, using the flow rate and activation time of the device, the microprocessor determines the dosage and can perform monitoring and reporting actions based on the dosage. A measuring circuit measures fluctuations in resistance/impedance of a vaporization element to further determine flow rate and/or dosage.

Abstract: Provided is a filtering facepiece respirator. The respirator includes a mask body having an anterior side portion, a posterior side portion, a middle portion, a first side portion, a second side portion, a top side portion, a bottom side portion and outer edge portions. The respirator further includes a primary port positioned at the anterior middle portion of the mask body and a detachable primary port adapter which is positioned over and engages the primary port. The respirator may further include an oxygen port and oxygen port adapter and a luer port and luer port adapter.

Abstract: Containment units, dry powder inhalers, delivery systems, and methods for the same are disclosed. Exemplary devices are configured to have inlets and outlets which are formed with the containment walls of a containment unit. Air jets formed by the configuration of inlet(s) and outlet(s) inside the containment unit create significant turbulence and deaggregate the powder. Delivery system components downstream of the containment unit may integrate the exiting aerosol plume with a low flow nasal cannula air stream for delivery to a subject.

Abstract: A breathing mask includes a mask body unit and a container. The mask body unit includes a mask body having an inner surface configured to cooperate with a user's face to define an interior space therebetween, and two straps respectively connected to two opposite sides of the mask body. The container has a container body defining a chamber for receiving working liquid and formed with a plurality of vent holes for communicating the chamber with the interior space. At least one gas generating unit is connected to the container, and includes an electrolysis device disposed in a casing thereof for electrolyzing the working liquid into a hydrogen/oxygen gas mixture.