Abstract: A respirator assembly is composed of a respirator, an air purifier, and a connection tube. The respirator includes a first housing having an inflow unit and an air intake. A first pumping unit is located in the first housing for sucking the air through the inflow unit and exhausting the air through the air outtake. The air purifier includes a second housing having an air intake and an outflow unit. A second pumping unit is located in the second housing for sucking the air through the air intake and exhausting the air through the outflow unit. The outflow unit includes a natural-air outlet and a respirator outlet. The connection tube includes two ends, one of which is connected with the respirator outlet and the other is connected with the inflow unit. Accordingly, the respirator assembly can reduce the frequency of replacing the respiratory screen and enhance the quality of filtering the air.

Abstract: Systems, methods, and apparatus for removing volatile anesthetics from an anesthesia or ventilation system to minimize the effects of malignant hyperthermia in susceptible patients. According to one aspect of the present invention, a system for removing volatile anesthetics is provided. A first filter component placed in fluid communication with an inspiratory limb of an anesthesia or ventilation system such that volatile anesthetics will pass through the first filter component during operation of the anesthesia or ventilation system. A second filter component is operably coupled to the expiration port of the anesthesia or ventilation system such that gases passing through the expiratory limb of the anesthesia or ventilation system pass through the second filter component. The first filter component and second filter component are adapted to effectively remove volatile anesthetics passing through the respective filters.

Abstract: An emergency oxygen mask includes: a respiration part worn on a user's face for supplying oxygen or discharging carbon dioxide or moisture using a pressure difference depending on respiration of the user; a carbon dioxide supply part for supplying the carbon dioxide and the moisture discharged from the respiration part through a carbon dioxide supply hole at a lower surface of the carbon dioxide supply part; an oxygen generating part engaged with an outer surface of the carbon dioxide supply part and having an upper open surface for reacting potassium dioxide in the carbon dioxide supply part with carbon dioxide or moisture to generate oxygen; an oxygen storage part for storing oxygen moved by an oxygen moving part; and filters attached to opposite sides of the oxygen moving part to remove carbon dioxide remaining in the oxygen stored in the oxygen storage part and to lower the temperature and humidity of the oxygen supplied to the respiration part.

Abstract: In a method and device for reducing the carbon dioxide content in a dead volume intended for connection to the respiratory system of a patient, and an anesthesia apparatus embodying such a device, a flow of gas is generated from an outlet associated with the dead volume and the gas is conducted through a carbon dioxide absorber, and the gas after passing through the carbon dioxide absorber is returned to an inlet associated with the dead volume.

Abstract: An adapter for connecting, in particular, respiratory implements such as tubes, tube extensions, filters, breather bags, or artificial noses to a tube having a particularly conically tapered connector. the adapter has a clamping section that may be fixed to the connector in a frictionally engaged manner. The clamping section of the adapter may be radially expanded from a first clamping position in which the inner diameter of the clamping section is less than the outer diameter of the connector into a second release position in which the inner diameter of the clamping section is greater than the outer diameter of the connector.

Abstract: Described herein are nasal respiratory devices, in particular, nasal respiratory devices configured to achieve positive end-expiratory pressure (PEEP) in a subject wearing the device. PEEP devices may have a threshold pressure for opening during expiration. In some variations, these devices have a threshold pressure for closing during expiration.

Abstract: A closed circuit rebreather including a breathing hose assembly, head assembly and internal counterlung assembly having axial and radial gas flow passageways therethrough, wherein the assembly is housed within a tank and includes a scrubber substantially enclosed along its longitudinal length within a water impervious counterlung bladder, the scrubber including foraminous inner and outer tubes having a carbon dioxide absorbent material filling the space therebetween.

Abstract: A breathing apparatus is operable in self-contained and filtered modes of operation. In the self-contained mode of operation, a breathable gas is delivered to a user from a self-contained source of breathing gas. In a second, filtered mode of operation, a suction source draws ambient air through a filter removing contaminants and delivers filtered ambient air to the user. A method of delivering air to a subject is also provided.

Abstract: A modular powered air purifying respirator (PAPR) which is comprised of a fan, motor, scroll, and power source mounted within one housing, and which accepts either traditional or conformal filters. Ambient air is drawn into the PAPR module through the attached filter by a fan, which is driven by direct connection to a motor. The pressurized air is then accelerated by an optimized scroll to the outlet in the PAPR housing. The PAPR module can be employed in multiple use configurations. The PAPR module further comprises a removable battery pack module that is easily retained to/removed from the PAPR module, enabling a user to be able to quickly remove a spent battery pack module and install a fresh battery pack module, thereby replacing the batteries within one breath cycle.

Abstract: A breath condensate sampler for use with a mechanical ventilator, the breath condensate sampler includes an airflow valve, a condensate formation tube, a condensate trap, and a condensate collection receptacle. The airflow valve directs air from the expiratory limb into the condensate formation tube wherein the condensate portion of exhaled gases are separated from the gaseous portion of the exhaled gases. A method of collecting a breath condensate sample is also herein disclosed.

Abstract: A ventilatory support and resuscitation device for providing short-term ventilatory support, as well as constant flow, pressure cycled ventilatory support for breathing and non-breathing patients is disclosed. The device includes a chamber and at least one port in flow communication with the chamber. The apparatus also includes a flexible diaphragm member positioned within the chamber and configured to seal the port from flow communication with the chamber while seated adjacent to the port, and to flex in response to pressure applied thereto so as to allow flow communication between the port and the chamber while the diaphragm is flexing. A flow restrictor in flow communication with the chamber may also be included. The device may be coupled to a patient adapter, whereby a manometer, entrainment unit, and safety pop-off and entrainment valve may be coupled thereto.

Abstract: The present system is an adsorption system for separating air into a concentrated gas component, which has an air supply, a compressor for receiving and compressing the air supply, providing a compressed air supply, and molecular sieve material for separating the compressed air supply into a concentrated gas component. The adsorption system delivers at least 5 liters per minute (LPM) of concentrated gas component from the molecular sieve material in which the system has a specific total weight per LPM <9 lbs/LPM. Additionally, an output quantity of the concentrated gas is delivered by the adsorption system and a purging quantity of the concentrated gas is dispensed into a sieve chamber of the adsorption system undergoing a purge cycle. The purging quantity has a value equal to or less than the difference between the maximum quantity and the output quantity, and the purging quantity is controlled based on the output quantity.

Abstract: An improved carbon dioxide absorber for use in a closed circuit patient breathing system has a canister insertable in the breathing circuit for receiving recirculating breathing gases. The canister contains a pelletized CO2 absorbent material that removes the CO2 from the breathing gases passing through the absorber. A quantity of the CO2 absorbent material is treated with a chemical indicator such that the chemical indicator makes a color change indicative of the state of the absorptive capacity of the absorbent material. A separate quantity of the CO2 absorbent material is treated with a second chemical indicator. The second chemical indicator changes color to indicate the degree of dryness of the CO2 absorbent material. The second chemical indicator may comprise cobalt chloride and serves to indicate the potential for excessive heat generation and toxic gas generation conditions within the CO2 absorbent canister.

Abstract: The present invention relates to an apparatus and process for oxygen concentration that makes possible the production of highly purified concentrated oxygen by modifying the structure of the adsorption bed and with various valves coupled thereto, and which can increase purity of the oxygen produced and reduce mechanical energy and consumption of electricity of the air compressor.

Abstract: The present invention provides a gas-delivery system for delivering breathable gas to a subject, comprising a source of pressurised gas, a mask cushion, a means for positioning the mask cushion for delivery of gas, and a filter for filtering particles from exhaled air. Preferably, the filter filters exhaled air only. The filter may engage a mask frame on any suitable surface of the frame in relation to the mask cushion.

Abstract: A combined air-supplying/air-purifying breathing system that includes a self-contained breathing apparatus, a facepiece for delivering breathable air from the self-contained breathing apparatus to a user, and a powered air-purifying respirator having at least one filter and a blower and having an output connected by a hose assembly to the facepiece. A control interface operationally connects the self-contained breathing apparatus to the powered air-purifying respirator. The self-contained breathing apparatus includes a pressure vessel, a cylinder valve assembly and a pressure reducer, all carried by a back frame, and the powered air-purifying respirator is adapted to be mounted on, and carried by, the back frame, by coupling the back frame and the respirator together at respective attachment points.

Abstract: The present invention is embodied in a portable self contained ventilating appliance, including an interface device coupled to at least one of an oral cavity or nasal cavity of a user, a ventilation device physically extending from the interface and configured to deliver pressurized air to the user through the interface, and a sensor monitoring system coupled to the interface and the ventilation device and configured to monitor the user.

Abstract: A compressor suitable for use in a portable oxygen concentrator. In one exemplary embodiment, the compressor includes a crankshaft rotatable about a central axis and a plurality of diaphragm assemblies spaced apart around the central axis generally within a plane. The diaphragm assemblies include diaphragms movably mounted to respective housings to at least partially define chambers. A plurality of rods extend between respective diaphragms and the crankshaft. The rods are coupled to the crankshaft such that the rods are offset axially from one another along the central axis and are coupled to the diaphragms for cyclically increasing and decreasing pressure within the chambers as the crankshaft rotates about the central axis.

Abstract: The invention relates to a gas supply unit (1) for supplying pressurised gas to a patient (8), wherein it comprises: —A pneumatic housing (10) for supplying a flow of gas to the patient (P), • A control housing (20) for controlling the flow of gas to be supplied to the patient (P), and A power supply housing (30) for supplying power to the unit (1), wherein the three housings (10,20,30) are distinct from one another and are designed for being removably coupled together to form a single unit (1). It further relates to a respiratory System for supplying a patient (P) with pressurised gas, the System comprising such a gas supply unit (1).

Abstract: A portable gas fractionalization apparatus that provides oxygen rich air to patients is provided. The apparatus is compact, lightweight, and low-noise. The components are assembled in a housing that is divided into two compartments. One compartment is maintained at a lower temperature than the other compartment. The lower temperature compartment is configured for mounting components that can be damaged by heat. The higher temperature compartment is configured for mounting heat generating components. An air stream is directed to flow from an ambient air inlet to an air outlet constantly so that there is always a fresh source of cooling air. The apparatus utilizes a PSA unit to produce an oxygen enriched product. The PSA unit incorporates a novel single ended column design in which all flow paths and valves can be co-located on a single integrated manifold. The apparatus also can be used in conjunction with a satellite conserver and a mobility cart.

Abstract: An air recycling device for auxiliary respiration apparatus has a casing, an air gather assembly, a valve assembly and a pressure switch unit. The casing has a regulator connector and an air feeder. The air gather assembly communicates with the casing. The valve assembly selectively blocks the communication either between the air feeder and the air gather assembly or between the regulator connector and the air feeder. In the moment between inhaling and exhaling, the pressure switch unit drives the valve assembly to block the communication between the air feeder and the regulator connector to gather the air expired from the user into the air gather assembly. When the user inhales again, the user inhales the air in the air gather assembly. The subsequently expired air flows through the regulator connector to a diving regulator. The air expired by the diver is recycled.

Abstract: Component gas is separated from a gas mixture. Component gas flow rate, or demand, is determined. One or more gas separator operating parameters is changed based on the component gas flow rate. For example, gas flow rate can be approximated by measuring a rate of pressure decay of a product tank during a time period in which the tank is not being replenished by the separating system. When it is determined that the flow rate is relatively low, operating parameters of the separating system are changed to improve system performance with the lower demand. For example, a target product tank pressure at which sieve beds are switched can be lowered when demand is lower.

Abstract: A medical device and method for combination lung ventilation and mucus clearance of a patient is disclosed. The medical device may be configured to provide lung ventilation with intermittent, on-demand mucus clearance, freeing the patient's mouth for activities of daily living such as when the patient is awake; and, in another configuration, the device can provide lung ventilation with automated mucus clearance, such as when the patient is sedated or asleep. The medical device may comprise a pressure generation source, a ventilation portion, and a mucus clearance portion. The mucus clearance portion may be separable from or separate from the ventilation portion such that the medical device is capable of maintaining lung ventilation with the mouth interface removed from the patient.

Abstract: PSA process for oxygen production comprising (a) providing an adsorber having a first layer of adsorbent selective for water and a second layer of adsorbent selective for nitrogen, wherein the heat of adsorption of water on the adsorbent in the first layer is ?about 14 kcal/mole at water loadings ?about 0.05 to about 3 mmol per gram; (b) passing a feed gas comprising at least oxygen, nitrogen, and water successively through the first and second layers, adsorbing water in the first layer of adsorbent, and adsorbing nitrogen in the second layer of adsorbent, wherein the mass transfer coefficient of water in the first layer is in the range of about 125 to about 400 sec?1 and the superficial contact time of the feed gas in the first layer is between about 0.08 and about 0.50 sec; and (c) withdrawing a product enriched in oxygen from the adsorber.

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: A novel and non-obvious apparatus, system, and method for managing respiratory secretions and fluids in sections of artificial airways. In an embodiment of the invention, a respiratory secretion retention (RSR) device configured to connect to an artificial airway can be provided. The respiratory secretion retention (RSR) device can include a housing that defines a passageway for the flow of respiratory gases, a chamber that is defined by the housing, where a portion of the chamber is configured to retain exhaled respiratory particulate and liquid, and at least one element configured to provide for repositioning at least a portion of the housing with respect to the artificial airway. In an aspect of this embodiment, the at least a portion of the housing can be repositioned with respect to the artificial airway without opening the artificial airway to the atmosphere.

Abstract: Breathing responsive powered air purifying respirator apparatus comprising an air-tight housing having connections for filters (5) and for supply of purified air to a face mask (3), a motor-driven blower arranged inside said air-tight housing for drawing air through said filter units and for the supply of purified air to the face mask. The blower is a lobe blower (6) delivering a constant flow of air. A regulator (10) is arranged in said housing in parallel with the lobe blower (6), and a by-pass conduit (11) connects the outlet side (12) of the lobe blower to the inlet side (13) of the lobe blower, wherein said regulator is arranged to open said by-pass conduit, when a pressure in the face mask exceeds a predetermined positive pressure.

Abstract: An electronic controller (16) controls the operation of an electrochemical oxygen generating system (14) producing a desired gas. The product gas is fed to a storage unit (12) or a regulator (28) and pulsing valve (28) controlling the gas flow to a user. A two-stage system (180) combines a low pressure 100 and a high pressure (150) gas generating subsystems. The low pressure subsystem (100) uses IMAT's (106) to pump oxygen from ambient air to generate a low-pressure. The high pressure subsystem (150) uses IMAT's (160) to pump oxygen to high-pressure oxygen storage devices (194).

Abstract: The apparatus is equipped with cover unit (1) fixed to a head portion of worker so as to cover at least the regions of nose and mouth of the worker, the cover unit capable of trapping the worker's breath. The cover unit has an exhaust opening and an air supply opening. Further, the apparatus is equipped with moisture recycle unit (2) fitted to the worker so as to simultaneously carry out the two processes consisting of the adsorption process of introducing moist air, effecting adsorption of the water contained in the air on an adsorbent and emitting dry air and the regeneration process of introducing dry air, effecting evaporation of the water adsorbed on the adsorbent into the dry air and emitting moist air. Still further, the apparatus is equipped with exhaust hose (3) connecting the exhaust opening of the cover unit to the moisture recycle unit and with air supply hose (4) connecting the moisture recycle unit to the air supply opening of the cover unit.

Abstract: An oxygen concentrator system that includes or can be expanded to include more than one compressor is provided. The system utilizes a controller that is adapted to selectively activate or deactivate one or more of the compressors to optimize system performance and efficiency. Multiple compressors can be selected to operate at the same time, thereby enabling the system to operate at a higher peak pressure, increase the recovery of the PSA cycle, and expand the product rate. The additional compressors can also be removed when not in use so as to reduce weight of the system. In some implementations, the system housing reserves a certain amount of space for accommodating additional compressors and related components, which can be added to the system as after market parts. In other implementations, the additional compressor can be located external to the system.

Abstract: An oxygen concentration apparatus (300) according to the present invention has: pressure swing adsorption type oxygen concentration means (310); and a control means (350) that controls switching means (316) that switches between intake of pressurized air into an adsorption column (312) and exhaust from the adsorption column. The switching means is controlled based on pressure in oxygen concentrated gas in the conduit measured by pressure measuring means to adjust a cycle of adsorption and regeneration processes of the oxygen concentration means so that pressure at the upstream of flow rate adjusting means (340) can be controlled and, as a result, the need for a mechanical pressure regulating valve, that has been needed conventionally, can be eliminated.

Abstract: A compressed air respirator with prolonged operating time due to rebreathing. The compressed air reservoir includes a compressed air reserve with a connected demand air supply valve, a reversible breathing gas reservoir (4) with a registering device (5) detecting the filling level of the breathing gas reservoir (4), and with an inspiration and expiration line (7, 8) for the user of the apparatus. A valve (6) is connected with the inspiration and expiration line (7, 8) and, on the inlet side, with the compressed air reserve (1) with a demand air supply valve (2) and with the breathing gas reservoir (4) and, on the outlet side, with the ambient air (11) and with the breathing gas reservoir (4).

Abstract: A method and apparatus are disclosed for recovering and separating anesthetic gas components from waste anesthetic gases to be purged from a healthcare facility. Prior to a condensation step, a compressor is used to increase the waste anesthetic gas pressure in order to facilitate condensation of anesthetic gas components at higher temperatures and in greater amounts than through condensation at lower pressures. Condensing the anesthetic gas components from the compressed waste anesthetic gas stream is then achieved using conventional condensation systems, which remove anesthetic gases as either liquid condensates or solid frosts. A preferred embodiment of the invention may be used with existing high-flow scavenging or reclamation systems but is more preferably used with low-flow scavenging or reclamation systems, which employ intelligent waste anesthetic gas collection units to minimize the ingress of atmospheric gas when no waste anesthetic gas is to be purged from the healthcare facility.

Abstract: A ventilator system is disclosed herein. The ventilator system includes a collapsible reservoir assembly comprising an outer reservoir and an inner reservoir disposed at least partially within the outer reservoir. The ventilator system also includes a source of gas pneumatically coupled with the outer reservoir, and a controller operatively connected to the source of gas. The controller is configured to regulate the transmission of gas from the source of gas to the outer reservoir in order to compress the inner reservoir and thereby automatically transfer the contents of the inner reservoir.

Abstract: The present invention provides a method for improving the air quality in the limited space and the equipment using thereof. The said method is that the air suctioned from the limited space is transferred to the outside of the limited space and acts as an air source for making oxygen. The oxygen is extracted from the said air source and the waste gas generated thereby is directly discharged to the outside of the limited space. The oxygen extracted is transferred into the limited space and offered the said space by means of the oxygen-supply controller. In addition, the atmosphere is supplemented into the limited space when the air inside is suctioned out. The equipment for the said method includes an indoor machine positioned in the limited space, an outdoor machine and an atmosphere supplement equipment.

Abstract: A powered air-purifying respirator that includes an enclosure, defining a single contiguous enclosed interior, an inlet duct, including an inlet and a distribution portion, that guides ambient air to the interior of the enclosure, a plurality of filter canisters disposed within the interior of the enclosure, and a blower that forces air through the at least one inlet, into the interior of the enclosure and through the plurality of filter canisters to produce filtered air suitable for breathing. A valve controls the flow of ambient air through the inlet duct. A fluid dam, disposed in an air path between the inlet and the filter canisters prevents liquids from reaching the filter canisters. The enclosure is reinforced and is adapted to provide protection for the filter canister from flame and heat while the filter canister is in use. A recirculation valve recycles previously-filtered air back into the enclosure.

Abstract: Oxygen breathing devices, as well as methods of providing oxygen to passengers or crew members of aircraft, are detailed. The devices may include an oxygen flow path with an oxygen buffer connected thereto.

Abstract: A breathing apparatus is operable in self-contained and filtered modes of operation. In the self-contained mode of operation, a breathable gas is delivered to a user from a self-contained source of breathing gas. In a second, filtered mode of operation, a suction source draws ambient air through a filter removing contaminants and delivers filtered ambient air to the user. A method of delivering air to a subject is also provided.

Abstract: A method and apparatus are disclosed for recovering and separating anesthetic gas components from waste anesthetic gases to be purged from a healthcare facility. With minimal reliance on the utility infrastructure and supplies of a healthcare facility, the method and apparatus needs only electrical or mechanical power, a source of waste anesthetic gases, and an atmospheric vent in order to operate. A heat exchanger/condenser, which uses a dedicated heat transfer fluid as a refrigerant, is employed to condense anesthetic gas components from the waste anesthetic gases as either liquid condensates or solid frosts. The warmed heat transfer fluid is cooled in a separate refrigeration unit and recycled back to the heat exchanger/condenser. A preferred embodiment of the invention is a self-contained, packaged unit which can be easily accommodated in a physician's office, small animal clinic, dental office or other healthcare facility requiring effective waste anesthetic gas management.

Abstract: A rapid cycle pressure swing adsorption oxygen concentration method uses a mechanical valve that has at least one cam-actuated flow control valve to switch flow of fluid, such as compressed air coming into a sieve tank that is fitted with molecular sieve materials. The cam-actuated flow control valve is repeatedly actuated by the rotating cams to become open or closed to complete a cycle that precisely controls the flow direction, pressure conditions and pressurized timing in the sieve tank whereby performance and efficiency of producing rapidly oxygen is high.

Abstract: A powered air purifying respirator includes a housing defining an air inlet and an air outlet; a filter assembly operably connected to the housing for removing contaminants from air passing therethrough; an impeller/motor assembly contained within the housing for drawing air through the air inlet and through the filter; a flow sensor contained within the housing for measuring air flow from the air inlet to the air outlet; and a liner contained within the housing for locating and retaining the various internal components, while also aiding in attenuating a force of impact to the housing, the liner further defining an air pathway from the impeller/motor assembly through the flow sensor and to the air outlet.

Abstract: An adsorbent is described. The adsorbent may include a membrane and an adsorbent material encapsulated within the membrane. An inhalation device is also described. The inhalation device may include a housing and a membrane within the housing. The membrane may encapsulate an adsorbent material. The membrane may be positioned such that airflow through the housing passes across but not through the membrane.

Abstract: A medical breathing apparatus incorporating a regulator for supplying breathing gas to a patient from an air hose (11). The regulator supplies breathing gas on demand to the patient via a mouthpiece or similar attached to an output connector (55). The connector forms part of a removable output unit (4) incorporating a filter (53) and an exhale flap valve (57/58) on the patient side of the filter. When the patient exhales, exhaled gas entering the connector (55) exits to atmosphere via the exhale valve without passing through the filter into the interior of the regulator, thus reducing cross-contamination between patients. Also described is an improved valve seat (16)/valve member (18) assembly in which multiple spaced pivot points (22, 23) are defined to cause the mechanical advantage for operating the valve member to reduce as the valve opens, thus reducing the force needed to operate the valve at lower flow rates.

Abstract: An apparatus for reversing inhaled anesthesia includes a filter for removing one or more anesthetic agents from gases passing therethrough, as well as a component for elevating CO2 levels in gases that are to be inhaled by a subject. The CO2 level-elevating component facilitates an increase in the ventilation of the subject without resulting in a significant decrease in the subject's PaCO2 level and, thus, a decrease in the rate at which blood flows through the subject's brain. A method of reversing the effects of inhaled anesthesia includes increasing the rate of ventilation of an anesthetized subject while causing the subject to inhale gases with elevated amounts of CO2 and while filtering anesthetic agents from such gases.

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: A face mask assembly and method of assembling a face mask is provided for a patient that includes a face piece sized to fit over the patient's nose and mouth. The face mask assembly forms a mask chamber between the face piece and the patient's nose and mouth. An inhalation adapter is coupled to the face piece to deliver medication to the chamber. A filter housing is coupled to the face piece and includes a flange section that defines a passageway to connect the mask chamber and the flange section. A filter is positioned in the filter housing. A cover is coupled to the flange section and has an exhalation opening or vent to allow gases from the mask chamber to pass through the filter and escape from the passageway to the atmosphere. In a second embodiment, the filter housing is modified by providing a frame adjacent the bottom with a cross-shaped structure and a retainer button attached to the housing.

Abstract: A filter assembly for use in sidestream gas sampling assembly. The filter assembly of the present invention includes a hydrophilic member that is constructed from a porous material and is situated such that gas entering the filter assembly passes through at least a portion the hydrophilic member. In a further embodiment, the filter includes a hydrophobic member positioned downstream of the hydrophilic member. The hydrophobic member acts as a second line of defense against moisture reaching the sensing mechanism in the gas sampling assembly.

Abstract: A method and system for the fractionation and removal of nitrous oxide and other volatile halocarbon gas components from waste anesthetic gases using liquid oxygen are disclosed. Liquid oxygen is warmed for use in a healthcare facility by cooling and condensing waste anesthetic gases. A cold trap/fractionator is provided wherein selective components of the waste anesthetic gas are collected as a frost on the coils of the cold trap/fractionator by desublimation/deposition and/or condensation/solidification. In a periodic batch process, the collected frost is first thawed and the melted liquids or gases are then collected at various increasing temperatures, thereby separating the nitrous oxide and other halocarbon gas components by their varying melting points. The thawed anesthetic components are collected in separate tanks based on their melting points. Warmed by the waste anesthetic gases in the cold trap/fractionator, the oxygen is supplied to the healthcare facility for its normal uses.

Abstract: A practical, germicidal, personal protection system may be worn by a user to kill or deactivate germs, viruses or other pathogens, which are located in the air to be breathed by the user. Before entering a mask, a hood or a suit worn by the user, air is exposed, in a sterilization unit, to Ultra-Violet C-band (UVC) radiation. Advantageously, the UVC radiation is lethal to undesirable germs, viruses and other pathogens. In this manner, pathogen-free air may be provided to the user. Bulbs used to generate UVC radiation are known to also promote the creation of ozone. Accordingly, the personal protection system includes means to minimize the ozone in the air that ultimately reaches the user. A similar personal protection system may also be used expose, to UVC radiation, breath exhaled from the user, thereby killing any germs, viruses or other pathogens exhaled by the user.

Abstract: A barrier survival system that isolates a safe volume within a mine or other confined structure and provides breathable air to one or more survivors within the safe volume who are awaiting rescue by generating oxygen, removing one or more toxins, carbon dioxide and carbon monoxide; and providing heat.