Abstract: A liquid product storage and delivery system is provided. The liquid product storage and delivery system includes a storage tank and a liquid bladder supported inside of the storage tank.

Abstract: A high flow therapy system for delivering heated and humidified respiratory gas to an airway of a patient includes a respiratory gas flow pathway for delivering the respiratory gas to the airway of the patient by way of a non-sealing respiratory interface; wherein flow rate of the respiratory gas is controlled by a microprocessor, a mixing area for mixing a first gas and a second gas in the respiratory gas flow pathway, a humidification area downstream of the mixing area and configured for humidifying respiratory gas in the respiratory gas flow pathway, and a heated delivery conduit for minimizing condensation of humidified respiratory gas.

Abstract: A system for delivering breathing gas to passengers on-board an aircraft, including: a source of breathing gas, at least one face mask for passengers, a reservoir associated with each face mask, a delivery valve for each face mask, the delivery valve being disposed between the source of breathing gas and the reservoir, the reservoir being disposed between the delivery valve and the face mask, a sensor associated with each reservoir and configured to sense a filling of the reservoir, and a controller configured to control the delivery valve in a continuous supply mode to provide a continuous flow of breathing gas to the reservoir and to interrupt the continuous flow of breathing gas when the filing sensed by the sensor is a filling threshold.

Abstract: Disclosed is a nasal ventilation mask having separate ports to monitor end-tidal CO2 expulsion integrated into the mask in order to monitor end-tidal CO2 expelled nasally or orally. Also disclosed is a CPR mask for nose-to-mouth and/or mouth-to-mouth resuscitation, having a body shaped to cover the nose and/or mouth of a victim, the mask including a CO2 absorber for eliminating at least in part rescuer's exhaled CO2 delivered to the victim.

Abstract: A user interface convertible between a nasal configuration and an oral configuration. The user interface has a nasal cannula and a mouthpiece. The nasal cannula has a body portion and at least one prong extending from the body portion, the prong being adapted to direct a flow of gas into a nare of a user's nose. The mouthpiece is adapted to engage the mouth of the patient and direct a flow of gas into a user's mouth. In the nasal configuration the prong of the nasal cannula is adapted to direct a flow of gases into a nare of the patient. In the oral configuration, the nasal cannula is engaged with the mouthpiece such that a gases flow is provided to at least the mouth of the user.

Abstract: The present disclosure provides techniques for a ventilator system with a removable airway. A ventilator system may include a removable airway and a base unit. The removable airway may include an air inlet port, a patient inhalation port, an air exhaust port, a patient exhalation port, a first portion of a pressure sensor, and a first portion of a flow sensor. The base unit may include two pinch valves, a second portion of the pressure sensor, and a second portion of the flow sensor. In some cases, the airway does not comprise any openings other than the air inlet port, the air exhaust port, the patient inhalation port, and the patient exhalation port. In some cases, air inside the removable airway does not contact any part of the base unit without first exiting the air exhaust port.

Abstract: The invention relates to a valveless spacer device for a metered dose inhaler (MDI), the spacer device comprising a body having an inlet and an outlet opposed from the inlet, a demountable, flexible bag attached to the body, the bag and body together defining a chamber, such that the inlet and outlet are in fluid flow communication with an interior of the chamber, wherein the inlet is configured to be connected to an MDI containing a drug to be inhaled and wherein the flexible bag, following actuation of the MDI, serves as a reservoir allowing for the formation of a cloud or mist of the drug therewithin which is then ready for inhalation, the flexible bag being configured to be at least partially deflatable and at least partially inflatable commensurate with a single breath and/or rebreathing.

Abstract: Respiratory masks made of thermoformed EVA foam are provided. A mask can include a seal that contacts a user's face in use and a housing permanently joined to the seal. Both the seal and housing can be made of EVA foam. The seal and housing can be made of EVA foam having different densities. The mask can further include a frame removably or permanently coupled the housing. Headgear can be coupled to the frame and can couple the mask to the user's face in use.

Abstract: In at least one embodiment, a system includes an inhalation source; a plenum in fluid communication with the inhalation source; at least one challenge plethysmography mask in fluid communication with the plenum, for each challenge plethysmography mask including a mask having a cavity to receive at least a nose of a test animal, a delivery conduit in fluid communication with the plenum and the cavity of the mask, at least one exhaust conduit in fluid communication with the cavity of the mask and the plenum, and a pressure sensor attached to the mask to measure pressure within the cavity of the mask; at least one processor in electrical communication with the at least one pressure sensor, the processor configured to process an output signal of the pressure sensor into respiratory data for each test animal during an exposure study; and an exhaust system in fluid communication with the plenum.

Abstract: A respiratory device includes a blower having an inlet and an outlet, a patient interface, and a valve including a valve member that is rotatable through a first angular displacement in a first direction from a first position to a second position. The outlet of the blower is coupled to the patient interface so that positive pressure is provided to a patient's airway via the patient interface when the valve member is in the first position. The inlet of the blower is coupled to the patient interface so that negative pressure is provided to the patient's airway via the patient interface when the valve member is in the second position. The valve member is rotatably oscillated back and forth when the valve member is in the first position and when the valve member is in the second position so that oscillations in the positive pressure and negative pressure, respectively, are provided to the patient's airway.

Abstract: A buoyancy control device having a back panel and including at least one flotation bladder, which at least one flotation bladder is configured with the device for controllable inflation and deflation, and connected thereto a harness arrangement for securing the device to a body of a user, the device having a cylinder-mounting mechanism arranged to enable front or side mounting of at least one breathable gas cylinder is useful for snorkeling and diving or repeated diving from snorkeling. A particularly preferred configuration provides a lightweight device of less than 5 kg and an apparatus of no more than 10 kg whereby carriage to and from snorkeling and/or diving location is simplified.

Abstract: A diving mask includes a faceplate secured to a frame, a flexible skirt having a partition delimiting an upper viewing chamber from a lower breathing chamber, a snorkel having an inlet channel for inhaled air and at least one escape channel for exhaled air, the snorkel being a continuation of the upper part of the frame, the inlet channel for inhaled air leading into the upper chamber, whilst the first escape channel for exhaled air communicates with the lower chamber. The frame is rigid and inside the frame there is arranged at least one first inner duct for exhaled air having an upper end leading into the escape channel for exhaled air, and a lower end in fluid communication with the lower chamber.

Abstract: The invention relates to medical technology, to non-medicinal means for improving physical health and enhancing physical capabilities by means of a breathing system, and specifically relates to devices which are intended for inhaling hypoxic/hypercapnic mixtures having various compositions, and which have an adjustable resistance to inhalation/exhalation. According to a first variant, a breathing exerciser contains a first chamber, which is connected to means for connecting the exerciser to a user's respiratory tract; a second chamber, communicating with the first chamber; a third chamber, communicating with the second chamber; means for adjusting the composition of a breathing mixture; and means for adjusting the resistance to inhalation/exhalation, installed in a channel through which the first chamber and the second chamber communicate.

Abstract: A patient interface system for delivering a gas to a patient includes a patient interface device that includes at least one inhalation valve and at least one exhalation valve. The system also includes a venturi device that has at least one port for connection to a gas source. The venturi device has at least one primary air entrainment window and at least one secondary air entrainment window which is downstream of the at least one primary air entrainment window. The inhalation valve is disposed between: (1) the main body and (2) the primary and secondary air entrainment windows of the venturi device. At least one of the primary air entrainment window and secondary air entrainment window includes a means for closing the respective window, thereby changing a degree at which the respective window is open and changing a flow rate of the air flowing through the respective window.

Abstract: The invention relates to a passenger oxygen mask for the emergency supply of oxygen in an aircraft, with a breathing bag which is provided on the entry side with a tube for the oxygen supply, wherein the tube and the breathing bag consist of polyurethane. The invention further relates to a breathing bag, with which a flow indicator is integrated into the connection piece.

Abstract: A mask system for delivering air pressurized above atmospheric pressure to the airways of a patient to treat sleep disordered breathing (SDB) by continuous positive airway pressure (CPAP) may include a mask having a cushion configured to form a seal with the patient's nose; two inlet conduits, each of the two inlet conduits configured to extend from a position superior to the patient's head and along a corresponding side of the patient's head, and each of the two inlet conduits being in fluid communication with a corresponding side of the mask to deliver pressurized air to the mask; a first vent arrangement configured to be positioned superior to the patient's head in use and configured to discharge gas to atmosphere during therapy; and a second vent arrangement configured to be positioned inferior to the first vent arrangement in use and configured to discharge gas to atmosphere during therapy.

Abstract: A breathing mask has a mask body surrounding a cavity that is open towards one side and is intended for coming into contact with a human face around the mouth and/or nose. A valve arrangement is provided in the mask body with an inspiration valve, for controlling the flow of gas from a port for a breathing gas feed device for providing a breathing gas into the cavity, and an exhalation valve for controlling the flow of gas from the cavity into the surrounding atmosphere. An emergency breathing valve, controlling gas flow from the atmosphere surrounding the breathing mask into the cavity, has a pressure threshold, to allow gas flow, that is lower than an inhalation valve pressure threshold. The pressure thresholds at which the respective inhalation valve and the emergency breathing valve open are coordinated by the closing element being designed as a separate component of the valve arrangement.

Abstract: A patient interface has a frame with an opening to receive pressurized gas; a cushion permanently co-molded to frame and defining a breathing chamber; an elbow assembly releasably snap-fittable to the frame with an audible click signaling secure attachment between the elbow assembly and the frame, the elbow assembly including a rotatable swivel elbow; headgear to support the patient interface on the patient's head; and a plurality of gas washout holes to allow escape of CO2 from the breathing chamber.

Abstract: A gas supply mask apparatus has low possibility that a gas rising in a mask main body will flow out from the upper end and the surrounding vicinity of the mask main body and give discomfort to the eyes of a mask wearer. In this gas supply mask apparatus, an angle formed between a direction in which a gas introduction opening faces and a virtual vertical plane facing right frontways falls within the range of 30° to 60° (preferably, the range of 35° to 55°, and more preferably, the range of 40° to 50°) when the mask main body is viewed right sideways.

Abstract: A ventilatory assist system and method are disclosed. The system comprises a tube for connection to a patient's airway, inspiratory and expiratory tube lumens connected to the tube, an inspiratory air source connected to the inspiration tube lumen, and a controller of air pressure in the expiratory tube lumen. The pressure controller is responsive to a physiological breathing signal representative of patient's inspiratory effort to allow air flow through the expiratory tube lumen during a patient's expiration phase, partially restricting the air flow through the expiratory tube lumen to a so minimum air flow during a patient's inspiration phase. During both respiratory phases, a unidirectional air flow is produced through the inspiratory and expiratory tube lumens to prevent air expired by the patient from being breathed again. The physiological breathing signal allows synchronization of the ventilatory assist with breathing efforts of the patient.

Abstract: A manually actuated, self-inflating bag valve mask provides users with a positive pressure ventilation device that reliably provides a proper tidal volume to the patient and controls the rate of ventilation of the patient. The bag valve mask is lightweight, compact, durable, and quickly deployable in the field. The device is preferably operable with one hand and can be configured for use in low-light environments.

Abstract: An emergency resuscitation apparatus with external air volume control includes a housing having top and bottom plates pivotally coupled so as to siphon air into an internal reservoir via an inflow port and propel air out through an outlet port to a patient. A volume control plate is coupled to the bottom plate externally adjacent a second end wall, the volume control plate having a plurality of volume selectors. An air volume limit arm is operatively coupled to the volume control plate and selectively movable between and coupled to a selected volume selector. A volume limiting flange associated with the volume limit arm are positioned in a common vertical plane with top plate such that the volume limit flange prevents upward movement of the top plate beyond the setting of the volume limit arm so as to regulate a quantity of air being expelled.

Abstract: A nasal breathing apparatus with multifunction has two nasal inserts and one tubular chamber. In one embodiment, the first nasal insert forms an airtight barrier inside one nostril for delivering gases. The second nasal insert does not block the other nostril and is for sampling gases. The tubular chamber is in fluid communication with the first nasal insert but not the second nasal insert and has an outlet for discharging and delivering gases and for providing continuous positive airway pressure and ventilation. In another embodiment, both nasal inserts form an airtight barrier in the corresponding nostrils. The first nasal insert is dedicated for delivering gases and the second nasal insert for sampling gases. The tubular chamber is in fluid communication with both nasal inserts and has an outlet for discharging and delivering gases and for providing continuous positive airway pressure and ventilation.

Abstract: A respirator device having an elastomeric sleeve is provided. In an exemplary embodiment, a respirator device as described herein includes a body including a receiver having an elastomeric sleeve and a filter cartridge that includes a rigid nozzle element. The elastomeric sleeve defines a channel, and the elastomeric sleeve is configured to deform around the nozzle element when the nozzle element is inserted into the channel.

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one valve element (3) for controlling the passage of gas from the second compartment (2) to the first compartment (1). The invention concerns also a breathing assistance apparatus comprising a source of NO gas, and said nasal cannula assembly (10) in fluid communication with said source of NO gas.

Abstract: The invention concerns a breathing assistance apparatus having a source of Nitric Oxide in fluid communication with a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one valve element (3) for controlling the passage of gas from the second compartment (2) to the first compartment (1). The invention concerns also a breathing assistance apparatus comprising a source of NO gas, and said nasal cannula assembly (10) in fluid communication with said source of NO gas.

Abstract: The invention concerns a nasal cannula assembly (10) adapted to deliver gases to a patient comprising a first compartment (1) and a second compartment (2) separated by a separation wall (6); a pair of nasal prongs (5) in fluid communication with the first compartment (1); the first compartment (1) comprising a first inlet (11) for introducing a first gas into said first compartment (1); the second compartment (2) comprising a second inlet (2) for introducing a second gas into said second compartment (2); and the separation wall (6) comprising at least one valve element (3) for controlling the passage of gas from the second compartment (2) to the first compartment (1). The invention concerns also a breathing assistance apparatus comprising a source of NO gas, and said nasal cannula assembly (10) in fluid communication with said source of NO gas.

Abstract: The present invention relates generally to an oral device, or mouthpiece, for delivering a fluid to the mouth or oropharynx of a user. In one embodiment, the oral device includes an intraoral portion, an extraoral portion, and an auxiliary support device that serves to stabilize the oral device. In various embodiments, the auxiliary support device may be configured with ear loops, a support band, a support frame and/or a support member. The intraoral portion generally includes at least one outlet port through which the fluid is delivered to the oral cavity or oropharynx. A method of dispensing a fluid using the oral device is also provided.

Abstract: Oxygen regulator (1) to deliver breathing gas in a cabin (10) of an aircraft comprising a first inlet (12) for pressurized breathing oxygen, a second inlet (14) for diluter gas, an outlet (16) to provide a breathing mixture to a user, and a regulation device adjusting the concentration of breathing oxygen in the breathing mixture. The regulation device comprises a emergency device (30) that adjusts the concentration of breathing oxygen in the breathing mixture as a function of a variation speed of the cabin altitude.

Abstract: A breathing system is provided that employs a reservoir for holding oxygen or an oxygen and medicine mixture while the patient is not inhaling. The reservoir generally prevents waste and reduces cost and helps prevent the patient from re-inhaling the previously exhaled gases.

Abstract: A method and apparatus is provided to separate Platelet Rich Plasma (PRP) utilizing standard whole blood harvesting techniques and separating the solution via centrifugation preparation. A pump is provided to pump PRP/Stem Cell solution from a centrifugation reservoir in to a nebulizer to aerosolize the PRP/Stem Cell solution in the nebulizer with oxygen. A patient will then inhale the aerosolized or vaporized PRP/Stem Cell solution into their respiratory system. Removal of any waste PRP/Stem Cell solution is provided by trapping the PRP/Stem Cells and any other biological matter other in a HEPA filter and allowing exhaled gasses to safely exit the from the Semi-Rebreathing Chamber.

Abstract: A circulation system for use in a rebreathe system includes a base and a fan assembly coupled to the base. The base includes a motor and a rotatable drive shaft coupled to the motor. The fan assembly includes a housing with an inlet and outlet. The fan assembly further includes a fan coupled to the drive shaft to rotate therewith and is fluidly isolated from the drive shaft.

Abstract: Examples of the invention include inhalation systems, breathing apparatuses, and methods for administering a solution by inhalation to a patient. Example breathing apparatuses described herein may be configured to minimize loss of the solution to the environment. Additionally or instead, example breathing apparatuses may be configured to recirculate exhaled solution to increase an amount of the solution available to a patient while minimizing exhausted solution. In some examples, breathing apparatuses may deliver nebulized platelet rich plasma (“PRP”).

Abstract: A manual emergency resuscitator uses a volume control system having pre-defined setting to accommodate patients of different sizes. An upper plate 305 is attached to a front hinge assembly 103 and a lower housing assembly is attached to the front hinge assembly. The lower housing assembly defines the lower portions of an accordion chamber 206. A selection void 300 is defined within the upper plate 305, with the selection void further defined by voids indexed to a closed position, infant position, child position and an adult position. A volume selector cord 201 has a first end attached to a volume selector, with the volume selector contained within the selection void. Placing the volume selector into one of the predefined positions regulates the amount of air delivered by the resuscitator.

Abstract: A manually operated ventilating element such as a bellows for administration of artificial respiration, for example, during anesthesia, has wall sections or pleats of different diameters. When the element is actuated through a small stroke length, the smaller section is actuated. A small volume of gas is delivered and the change in delivered volume per unit stroke length is small, so that the operator can precisely control the delivered volume. When the element is actuated through a larger stroke length, a larger volume per unit stroke length is delivered. The same element can be used to treat children and adults.

Abstract: An aspiration and resuscitation system which is useable to perform aspiration and/or resuscitation procedures on living beings, particularly small animals, and most particularly newborn small animals such as puppies and kittens. The system includes an aspirator and a resuscitator. Each includes a separable pump and animal interface mask. Further disclosed are aspiration and resuscitation methods using the disclosed apparatus.

Abstract: A spirometer-type device is described that is designed to improve patient compliance with therapeutic breathing for improved pulmonary function. In an example embodiment, a display of human lungs is provided that visually elevate with inhalation. A patient's progress is visualized with a featured conspicuous level marker and upward motions of lungs that are seen from both sides of the device.

Abstract: A gas assisted re-breathing device is provided for life support of individuals venturing into harsh environments, particularly the underwater environment, which results in reduced work of breathing. In the pressurized gas assisted re-breathing device, pressurized gas, actuated by the breathing pressure local to the mouthpiece, acts to move a flexible gas storage container on behalf of the individual and a loop seal valve is forcibly shut during assisted breathing, which seals the assisted breathing loop to prevent premature venting of breathing gas to the surrounding environment, unless the assisted breathing loop is full, whereupon the loop seal valve opens to allow excess breathing gas to escape into the surrounding environment through forcible exhalation by the individual through one or more conventional one way valves that prevent backflow from the surrounding environment back into the loop.

Abstract: An emergency oxygen supply system for use on aircraft in the event of a loss in cabin pressure is configured for delivering allotments of oxygen and timing the delivery such allotments to each passenger so as maximize the efficiency of the transfer of such oxygen into the passenger's bloodstream. The delivery of each allotment is selected so that the entire allotment is available for inhalation into the region of the lung most efficient at oxygen transfer while the volume of the allotment is selected to substantially coincide with the volume of such region of the lung.

Abstract: A rebreathing apparatus has a clothing article wearable on a person. The clothing article defines a channel configured to be fluidly connected to at least one tube. The tube is configured to be fluidly connected to a mouthpiece. When the person exhales, the exhaled breath enters one end of the channel and passes through the channel while being scrubbed of CO2. When the user inhales, the scrubbed air is drawn from the channel.

Abstract: A CO2 measuring device for use in a high humidity environment typically found in re-breathing apparatus, especially underwater re-breathing apparatus, that allows commonly available CO2 gas detectors to function properly and further provides for remote, continuous and/or quantitative sensing of CO2. Under normal conditions found inside re-breathers, a 100% relative humidity condensing environment exists that prevents the use of commercially available CO2 detectors which typically require relative humidity to be less than about 90 to 95% for proper operation. A venturi mixing device is disclosed that is driven by pressurized makeup gases routinely added into the re-breathing loop, acting to draw and mix with a portion of the moisture laden gas from the re-breather environment, creating a combined gas mixture with relative humidity well within the operating range of commercially available CO2 detectors.

Abstract: A therapeutic face mask comprises a face-engaging portion and a single connector having a mask-engaging end and a single treatment-receiving end which has a single attachment mounting for detachably sealingly receiving a treatment attachment, such as an oxygen reservoir bag or a nebulizer. A one-way inhalation valve in the connector permits fluid flow from the treatment-receiving end to the mask-engaging end during inhalation and inhibits fluid flow in the other direction. The mask also includes a valve-governed exhalation port and an anti-asphyxia valve assembly configured to permit fluid flow from ambient to the face-engaging portion during inhalation only when inspiratory effort during inhalation exceeds fluid flow to the treatment-receiving end of the connector. Also provided is an oxygen reservoir bag having a neck shaped for removable coupling to a mating connector of a therapeutic face mask. An oxygen reservoir bag may have a metered-dose inhaler port defined in its neck.

Abstract: The breathing bag has an upper region; a lower region; a conduit for delivering exhaled air to the lower region and a conduit for withdrawing breathable air from the upper region. The device also has a baffle mounted therein for entrapping exhaled air in the lower region and for causing the exhaled air to remain in a low turbulence mode, for promoting a separation of oxygen and carbon dioxide from the exhaust air by stratification and for causing carbon dioxide to accumulate in the lower region of the bag. Consequently, the breathable air rising from the lower region of the bag has a higher oxygen content. In another aspect of the invention, a method for separating carbon dioxide and oxygen by stratification from exhaled air is also described.

Abstract: An oxygen supply system for an aircraft includes a control valve, a reservoir bag, a respiration device and a sensor device, wherein the control valve is designed in such a way that oxygen can be supplied to the reservoir bag until a predetermined quantity of oxygen is adjusted in the reservoir bag. The respiration device may be designed in such a way that breathing gas can be provided for a passenger. The sensor device may be designed in such a way that an exhalation is detectable. The reservoir bag may be designed in such a way that a predetermined quantity of oxygen can be metered into the reservoir bag during the exhalation. The reservoir bag may be designed in such a way that breathing gas can be supplied to the respiration device in a pulse-like fashion. The oxygen supply system may include a first and a second operation mode.

Abstract: A breathing apparatus for ventilating the lungs of a patient with breathing gas, has: a breathing circuit configuration; a mechanical ventilation system; a manual ventilation system provided with a manual ventilation bag; a manual ventilation valve for enabling manual ventilation of breathing gas from the breathing circuit; a pressure sensor devised to detect the pressure level in the breathing circuit; an electronically controlled expiration valve (40) that in a mechanical ventilation mode is controlled to control the pressure level in the breathing circuit according to a first set of predetermined control rules adapted to mechanical ventilation mode requirements; said electronically controlled expiration valve in a manual ventilation mode being coupled to enable ventilation of breathing gas from the breathing circuit by means of the manual ventilation system according to a second set of predetermined control rules adapted to manual ventilation mode requirements.

Abstract: An adjustable volume control manual resuscitation bag assembly includes a resuscitation bag, a volume control knob, a traction assembly operating in response to adjustment of the control knob, and a follower assembly including a bag compression limiting member and a follower which are moved in response to operation of the traction assembly to adjust and limit the volume of gas delivered by compression of the bag.

Abstract: The function of a respiration system, with a patient port (1) with connected inspiration branch (3) and expiration branch, is checked. A rebreathing line (9) connects the inspiration branch to the expiration branch. A reservoir (25) is connected to a reservoir port (27) in the rebreathing line. An actuatable control valve (29) is provided in the rebreathing line between the expiration branch and the reservoir port. A pressure sensor (33) is connected to the rebreathing line. A control unit (39) is connected to the control valve and to pressure sensor. The process includes closing the control valve for a preset inspiration time and opening it for a preset expiration time. The value sent by the pressure sensor is detected with the control valve opened during the expiration time and compared with a preset first threshold valve. An error message is generated when the value sent exceeds the first threshold value.