Abstract: The present disclosure provides a control body adapted for use in an electronic smoking article. The control body includes a shell and a coupler that is adapted to connect the control body to a cartridge of an electronic smoking article. The coupler further is adapted to communicate a pressure reduction within the coupler to a pressure reduction space in the shell. Also positioned within the shell is an electronic circuit board having a pressure sensor attached thereto. The electronic circuit board can be positioned to be parallel to a central axis of the shell. A first end of the pressure sensor can be isolated within the pressure reduction space, and a second end of the pressure sensor can be in communication with a normal pressure space within the shell. One or more light emitting diodes can be attached to the electronic circuit board. At least a portion of the coupler can be light transmissive so that light from the LED is visible through the coupler.

Abstract: An electronic vaporizer including a heating element for heating a fluid to produce a vapor; a power source to provide electrical power to the heating element for heating the fluid; and a power control circuit configured to regulate a supply of electrical power from the power source to the heating element based at least in part on an operating temperature of the heating element and a temperature setting to prevent the operating temperature of the heating element from exceeding the temperature setting.

Abstract: A mask apparatus includes a mask body, a pair of hook mounting portions at side ends of the mask body, a seal coupled to a rear surface of the mask body, and a pair of ear hook portions connected to the hook mounting portions. Each hook mounting portion includes an upper hook mounting portion, a lower hook mounting portion below the upper hook mounting portion, a hook pin at each of the upper hook mounting portion and the lower hook mounting portion, and a through-hole defined in each of the upper hook mounting portion and the lower hook mounting portion. Each ear hook portion includes a strap portion, a first hook portion connecting the strap portion to one of the upper and lower hook mounting portions, and a second hook portion connecting the strap portion to the other of the upper and lower hook mounting portions.

Abstract: An elbow assembly for a patient interface includes a swivel component adapted to connect to a patient interface and an elbow component adapted to connect to an air circuit. The swivel component is coupled to the elbow component by a ball and socket joint and a hinge joint which allows the elbow component to pivot relative to the swivel component about a single axis.

Abstract: A medication inhalation apparatus preferably formed of a single, unitary sheet of stock, includes an outer housing, movable between collapsed and expanded states, encompassing a first volume. An inner housing within the outer housing encompasses an inner or second volume. An inhaler opening to the first volume is within a wall of the outer housing at a first location. A mouth opening to the inner volume is within a wall of the outer housing and the inner housing at a second location. A one-way inhalation valve connecting the first volume and the inner volume is within a wall of the inner housing. A one-way exhalation valve connecting the inner volume and the exterior of the outer housing is within a wall of the outer housing and inner housing at a third location. The valve preferably includes an elongated spring body formed of a semi-pliant material with a strength and rigidity providing limited flexibility.

Abstract: Disclosed is a connecting piece for artificial respiration. The connecting piece comprises an opening that faces a ventilation hose, an opening disposed toward a patient interface, and an opening to the atmosphere which can be at least partially closed from the inside by a diaphragm. The connecting piece further has a diaphragm opening for accommodating the diaphragm into the connecting piece, the diaphragm being held via a diaphragm ring that surrounds the connecting piece.

Abstract: The emergency oxygen supply for passengers in an aircraft comprises an oxygen source with a number of pulse breathing masks which are conductively connected to the oxygen source, wherein an individual shut-off valve which in the non-actuated condition is switched to block is provided in each conduit to a breathing mask. The emergency oxygen supply moreover comprises an impulse breathing control for actuating each individual shut-off valve, as well as an auxiliary conduit which connects the oxygen source to the breathing masks whilst bypassing the individual shut-off valves and which in each case via a check valve is connected to the respective conduit which leads to the breathing mask, or to the breathing mask itself. The auxiliary conduit is connected to the oxygen source via a central shut-off valve which is switched to open in the non-actuated condition.

Abstract: The present invention provides a respiratory mask comprising a nose cushion assembly. The nose cushion assembly comprises a base body and a buffering piece. The base body has a base intake portion, a base connection portion, and an air routing piece disposed at the inside of the base body and having a partitioning wall and a wall connection piece. The inside of the partitioning wall encloses an air intake zone. The wall connection piece is disposed outside the partitioning wall and connects with the base intake portion. Between the partitioning wall and the base intake portion there is defined an air outtake zone. The air intake zone is approximately at the center of the base intake portion. The buffering piece connects with the base connection portion and encloses a nose containing room, which in turn connects with the inside of the base body.

Abstract: A respiratory assembly is provided. The assembly includes a base engaged with at least one connector and in fluid communication with a hose or fluid source for allowing the gaseous flowthrough between the at least one connector, the base and the hose or fluid source. The assembly further includes a pair of sockets engaged with the at least one connector, and a pair of posts, each post selectively engageable with at least one of the pair of sockets. Each post includes a flange that defines an opening therethrough, the openings in fluid communication with each corresponding socket of the pair of sockets. Each post further includes an adhesive adhered to each flange and configured for sealably engaging a patient's nare.

Abstract: A respiratory mask connector and a respiratory mask. The respiratory mask connector is configured to connect a frame to a connection pipe. The respiratory mask connector has a connection face and a spherical face, the connection face being configured to be connected to the frame, and the spherical face being configured to be in ball-socket connection with a pipe head of the connection pipe. The connection face and the spherical face are respectively configured as either the outer wall surface of the respiratory mask connector or the inner wall surface of the respiratory mask connector. The respiratory mask connector can be used for a respiratory mask.

Abstract: A nebulizer assembly for a respiratory device is provided having a housing defining a chamber. The housing also has a nebulizer port configured to receive a nebulizer to discharge atomized medication into the chamber. An outlet of a handle is coupled to the inlet of the housing. A hose is coupled to an inlet of the handle. A patient interface is coupled to the outlet of the housing. Air flows from the hose to the patient interface via the handle and the housing. The air mixes with the atomized medication within the chamber.

Abstract: An attachable, detachable pressure reducing regulator for use with a primary high-pressure gas source, wherein the high-pressure chamber of said regulator includes a secondary gas IN portal, with a one-way valve, through which the primary container source may be refilled from an external gas source, via the high-pressure chamber of the said regulator, either independently of or concurrently during its use as a pressure reducing regulator.

Abstract: An oxygen supply system providing an adequate oxygen supply mode in an aircraft. A preventive oxygen supply system includes an oxygen source, a preventive oxygen dispensing unit connectable to the oxygen source, a cabin altitude detection device, and a preventive oxygen control device provide at least the following modes: a pre-wear mode providing no oxygen of the oxygen source to the preventive oxygen dispensing unit but normal cabin air; a pre-oxygenation mode providing a predetermined rate of oxygen of the oxygen source to the preventive oxygen dispensing unit sufficient for generating a pre-oxygenation condition of the user; and a decompression mode providing high concentrated oxygen of the oxygen source to the preventive oxygen dispensing unit sufficient for ensuring a minimum oxygenation of the user. The preventive oxygen control device automatically switches to the decompression mode in case a predetermined cabin altitude threshold is detected by the cabin altitude detection device.

Abstract: A medication inhalation apparatus includes an outer housing, movable between collapsed and expanded states, encompassing a first volume. An inner housing within the outer housing encompasses an inner volume. An inhaler opening to the first volume is within a wall of the outer housing at a first location. A mouth opening to the inner volume is within a wall of the outer housing and the inner housing at a second location. A one-way inhalation valve connecting the first volume and the inner volume is within a wall of the inner housing. A one-way exhalation valve connecting the inner volume and the exterior of the outer housing is within a wall of the outer housing and inner housing at a third location. In the expanded state, gas flows from the inhaler to the first volume, the first volume to the inner volume, and the inner volume to a user's mouth.

Abstract: The present invention relates to a tracheal ventilation apparatus, in particular a tracheostomy cannula or an endotracheal tube, having a cannula tube, which from a point of view from a gas supply, has a proximal tube portion with a proximal opening and a distal tube portion with a distal opening. In order to provide an easy-to-handle tracheal ventilation apparatus that can easily be inserted and that impedes a swallowing process as little as possible, the proximal tube portion and the distal tube portion are connected to one another by way of an axially air-permeable joint that facilitates at least restricted mobility and, in particular, pivotability of a longitudinal axis of the distal tube portion with respect to a longitudinal axis of the proximal tube portion.

Abstract: A medication inhalation apparatus includes an outer housing, movable between collapsed and expanded states, encompassing a first volume. An inner housing within the outer housing encompasses an inner volume. An inhaler opening to the first volume is within a wall of the outer housing at a first location. A mouth opening to the inner volume is within a wall of the outer housing and the inner housing at a second location. A one-way inhalation valve connecting the first volume and the inner volume is within a wall of the inner housing. A one-way exhalation valve connecting the inner volume and the exterior of the outer housing is within a wall of the outer housing and inner housing at a third location. In the expanded state, gas flows from the inhaler to the first volume, the first volume to the inner volume, and the inner volume to a user's mouth.

Abstract: Systems for use in assisted respiration can permit insertion of one or more elongated medical instruments into the proximal and/or distal airway of a patient during administration of assisted respiration, which may, in some instances, proceed with a patient awake or only minimally sedated. In some systems, a bite block is coupled with a mask and is movable relative to the mask such that the system is capable of accommodating differing patient anatomies.

Abstract: Methods and systems are provided for delivering anesthetic agent to a patient. In one embodiment, a system includes an anesthetic agent reservoir, a pump fluidically coupled to the agent reservoir, an injector configured to receive pressurized anesthetic agent from the pump, a vaporizer comprising a heated chamber configured to receive and vaporize the anesthetic agent injected by the injector and supply a mix of the vaporized anesthetic agent and medical gas to a subject via a supply line, and a controller. The controller stores instructions executable to determine a concentration of the vaporized anesthetic agent in the mix and adjust one or more injector parameters based on a difference between the concentration of the vaporized anesthetic agent and a commanded concentration.

Abstract: A gas sampling line having a channel for conducting respiratory gases from a patient respiratory interface to a gas monitor, the gas sampling line comprising, i.a., a gas sampling tube comprised of a polyether block amide material, the polyether segments of which comprise polyethyleneoxide. Use of a tube comprised of a polyether block amide material, the polyether segments of which comprise polyethyleneoxide, for sampling of respiratory gases; and a method for sampling of respiratory gases, the method comprising conducting respiratory gases through such a tube. A gas analysis system for analysing respiratory gases, comprising a gas sampling line as defined above and a gas monitor connectable to the gas sampling line.

Abstract: A respiratory treatment apparatus configured to provide a flow of breathable gas to a patient, including a breathable air outlet, an outside air inlet, and an pneumatic block module, wherein the pneumatic block module includes: a volute assembly including an inlet air passage, a mount for a blower and an outlet air passage; the blower being mounted in the mount such that an impeller of the blower is in a flow passage connecting the inlet air passage and the outlet air passage; a casing enclosing the volute assembly, wherein air passages within the casing connect air ports on the volute assembly, wherein the inlet air passage of the volute assembly is in fluid communication with the outside air inlet and the outlet air passage of the volute assembly is in fluid communication with the air outlet.

Abstract: An e-vaping device may include a pre-vapor formulation tank configured to hold a pre-vapor formulation, an adaptor that includes a vaporizer assembly configured to vaporize the pre-vapor formulation, and a flavor insert positioned to receive vapors formed by the vaporizer assembly. The flavor insert may hold at least one flavorant. The tank, adaptor, and flavor insert may be a non-combustible vaping element that includes a channel into which the flavor insert may be inserted to be positioned to receive the vapors. The flavor insert and the vaporizer assembly may be at opposing ends of the channel. The flavor insert may be a detachable insert configured to be inserted into the tank element. The flavor element may be a tobacco element. The tobacco element may be at least a portion of a cigarette.

Abstract: This non-combustion type flavor inhaler is provided with an atomization unit having an aerosol source and a resistive heating element for atomizing the aerosol source with resistive heat, and a control unit which controls the amount of power supplied to the resistive heating element, wherein the amount of power supplied to the resistive heating element during the action of a single puff is represented by E, characteristic parameters of the atomization unit are represented by a and b, the amount of the aerosol source consumed with one puff action is represented by L, and the control unit calculates L with the formula L=aE+b, or, controls E in accordance with the formula E=(L?b)/a.

Abstract: A connector or connector assembly for attaching a nasal cannula with a gas delivery hose includes a sensor port for a sensor probe positioned near an end of a nasal cannula, which can allow the sensor probe to be placed closer to the patient's nostrils than previous connector parts allowed. The connector assembly can be configured to automatically align locking protrusions on a first component with locking recesses on a second component, where insertion of the second component within the first component causes the second component to rotate relative to the first component, thereby aligning the locking protrusions with associated locking recesses.

Abstract: A patient interface used in a respiratory care system. The patient interface having an un-deflected configuration, a deflected configuration, and a formed configuration. The patient interface is adapted to elastically deflect, under the application of force, from the un-deflected configuration to the deflected configuration, and permanently deform when in the deflected configuration by mechanical creep deformation to the formed configuration.

Abstract: A fluid supply warning and communication system including fluid tight engagements being made with tubing having at least one connector end chosen from a universal connector, a twist-on nipple, and a v-shaped end. A gas supply warning and communication system including a first upstream gas path, a second upstream gas path, and a downstream gas path made with tubing having at least one connector end chosen from a universal connector, a twist-on nipple, and a v-shaped end. A method of increasing humidity in a downstream gas path in the gas supply warning and communication system by flowing gas through a downstream gas path tubing that increases humidity to an end use appliance.

Abstract: Component of a patient interface, particularly a cushion, comprising a first part and a second part, wherein the second part is made of a foamed material which is foamed-on the first part. A Method and tool for manufacturing a component of a patient interface, particularly a cushion, comprising the steps molding a first part of the component and foaming a second part on the first part.

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

Abstract: Full facemask including a face seal configured to directly engage a face of an individual. The face seal defines a lens opening. The full facemask also includes a mask lens that is coupled to the face seal and disposed within the lens opening. The mask lens has a passage edge that defines a cartridge passage through the mask lens. The full facemask also includes a cartridge module having at least one of a filter or an air regulator. The cartridge module is disposed within the cartridge passage and circumscribed by the passage edge of the mask lens. The full facemask also includes a locking member that includes a first member surface that directly engages the mask lens and a second member surface that directly engages the cartridge module. The locking member secures the mask lens and the cartridge module in fixed positions with respect to each other.

Abstract: A medication inhalation apparatus formed of a single, unitary sheet of stock, includes an outer housing, movable between collapsed and expanded states, encompassing a first volume. An inner barrier within the outer housing delineates a second volume. An inhaler opening to the first volume is within a sidewall of the outer housing at a first location. A mouth opening to the second volume is within a sidewall of the outer housing at a second location. A one-way inhalation valve connecting the first volume and the second volume is formed from a sidewall of the inner barrier. A one-way exhalation valve connecting the second volume and the exterior of the outer housing is formed from a sidewall of the outer housing and inner barrier at a third location. In the expanded state, gas flows from the inhaler to the first volume, the first volume to the second volume, and the second volume to a user's mouth.

Abstract: Embodiments relate generally to a self-contained breathing apparatus (SCBA comprising a waist pad bumper system. The waist pad bumper system may comprise a soft rubber gasket located between the waist pad and the backplate of the SCBA, operable to compress to cushion the movement of the backplate with respect to the waist pad; a hard rubber gasket located between the waist pad and the backplate operable to compress to cushion the movement of the backplate with respect to the waist pad; one or more magnets located on the waist pad; and one or more magnets located on the backplate operable to interact with the one or more magnets located on the waist pad, wherein the magnets of the waist pad have the same polarization as the magnets of the backplate and therefore repel each other.

Abstract: A portable device for checking wind direction discharges a visible, and optionally scented, vapor stream into the atmosphere in a well-defined reference direction. In some embodiments, the device includes a power source, a vessel having an internal plenum chamber storing a volume of air, a reservoir containing a vaporizable agent, a vaporizing element associated with the vaporizable agent, and a pressure switch. The vessel is deformable to generate an airflow that operates the pressure switch to temporarily connect the power source to the vaporizing element, thereby energizing the vaporizing element to generate vapor. The airflow also carries the vapor into the atmosphere as a visible vapor stream flowing in the reference direction. The reservoir and vaporizing element may be carried in a cartridge removably mounted on the device. Other embodiments operate similarly, but use alternative means for generating gaseous flow to operate the switch and/or carry vapor into the atmosphere.

Abstract: Inhalator (50) comprising an aerosol generator (64) configured to generate an aerosol by nebulizing a fluid and a controller (24) configured to control operation of the aerosol generator and a housing (11, 51) accommodating at least the aerosol generator and the controller, the housing having a base (12) for supporting the housing on a horizontal surface, wherein a portion (35) of the housing accommodating at least a portion of the controller is arranged further away from the base than the aerosol generator as seen in a vertical direction, when the base is supported on the horizontal surface.

Abstract: The present invention relates to an electronic smoking device, comprising a cell part (1), a cigarette body part (2) and a cigarette holder (3). The cigarette body part (2) comprises a shell (4) and a heating element (7) arranged within the shell (4). The heating element (7) comprises a tobacco container (5) in the shape of tube, and the cigarette body part (2) is provided with a through hole (17) which is connected to the tobacco container (5). The heating element (7) also comprises a heating unit (6); the heating unit (6) is sleeved on the outside of the tobacco container (5). The electronic smoking device of the present invention makes it possible to load and remove the tobacco conveniently, thus facilitating the cleaning of the tobacco container.

Abstract: A patient transfer device is configured for use with at least one host device which is capable of providing respiratory support to a patient. The patient transfer device includes an inspiratory port and an expiratory port which are configured to pneumatically connect to the host. An inspiratory connection is pneumatically connected to the inspiratory port and an expiratory connection is pneumatically connected to the expiratory port. An inspiratory valve is coupled between the inspiratory port and the inspiratory connection and expiratory valve is coupled between the expiratory port and the expiratory connection. The inspiratory valve and the expiratory valve are operable between first configurations that permit flow there though and second configurations that occlude flow through the valves. The inspiratory valve and the expiratory valve are configured to operate in the second configuration when the patient transfer device is disconnected from the at least one host device.

Abstract: A patient interface system for delivery of a supply of air at positive pressure to the entrance of a patient's airways for treatment of sleep disordered breathing includes an air delivery tube connected to a flexible portion of a plenum; a vent structure having sufficient rigidity to support its own weight under gravity and/or not to block or fold under tube movement or tube drag; and a patient interface structure. The patient interface structure includes a seal forming structure arranged on a top portion of the plenum; and a seal positioning and stabilizing structure connected to a flexible portion of the plenum. The seal-forming structure is substantially decoupled from a tube drag force.

Abstract: A cartridge for an e-vaping device includes an infrared sensor configured to measure infrared radiation emitted by at least a portion of a heating element coupled to a dispensing interface in the cartridge. The field of view of the infrared sensor may encompass an entirety of the heating element. The infrared sensor may be an infrared light emitting diode. The e-vaping device may include control circuitry configured to determine the temperature of the heating element based on sensor data generated by the infrared sensor and control the electrical power supplied to the cartridge based on the temperature of the heating element. The control circuitry may control the electrical power to maintain the temperature of the heating element below a threshold temperature. The control circuitry may determine the heating element temperature based on accessing at least a portion of the sensor data stored at a storage device in the cartridge.

Abstract: Disclosed is a suction device. The suction device includes a sensor unit configured to measure breathing condition of a patient, a tube unit configured to move into a bronchus of the patient so as to suck foreign material generated in the bronchus of the patient when a measured value measured by the sensor unit exceeds a predetermined reference value, and a control unit configured to control an operation of the tube unit based on the measured value measured by the sensor unit. According to the present invention, there is provided the suction device which is automatically operated by directly determining whether foreign material is generated in the bronchus of the patient.

Abstract: A swivel elbow and connector assembly for a patient interface system includes a ring configured to be sealingly secured in an aperture of the patient interface system. The ring includes a first side in an interior of the patient interface system and a second side at an exterior of the patient interface system when the ring is secured in the aperture. The ring also includes a plurality of vents configured to permit flow of gases from the interior to the exterior of the patient interface system. The swivel elbow and connector assembly includes an elbow swivelably secured in the ring. A patient interface system for delivering a flow of breathable gas to a user includes a patient interface structure configured to sealing engage the face of the user. The patient interface structure includes an aperture. A swivel elbow and connector assembly is sealingly secured in the aperture.

Abstract: A connector system for connecting a cable having a length to an item includes a base operatively connectible to the item, the base including a channel to seat at least a portion of the cable, the channel being in operative connection with the item upon connection of the base to the item, and a rotatable member which is rotatable relative to the base. The cable is in operative connection with the rotatable member so that, as the rotating member rotates relative to the base, a bend in the cable is formed at different locations in the length of the cable such that the different locations define different lengths of the cable. The different lengths of the cable become positioned within the channel as the rotating member rotates relative to the base.

Abstract: An adapter for use with a flow generator includes a conduit attachable to the outlet of the flow generator and an identifying element supported by the conduit and providing an identifying feature unique to a specific peripheral component attachable to the flow generator. The identifying feature is communicatable to the flow generator so that appropriate operating parameters of the flow generator may be automatically selected by the flow generator to coordinate with the specific peripheral component.

Abstract: A vaporizing device generally having a tank, power component, battery, and shroud is disclosed. The power component may include a frame defining a slot configured to receive the tank in an upright position, such that a portion of the tank is adjacent to the power component when the tank is in position. The battery may be coupled to the frame of the power component. The shroud may be configured to be positioned around the battery and coupled to the frame. The battery may be activated when the shroud is compressed radially inward. The device may include a port for connection to an external power supply for recharging the battery. The device may be portable with a generally compact configuration in order to allow a user to comfortably hold the device in the palm of the hand.

Abstract: A breathing mask arrangement includes an arch body, a sealing lip means for bearing against the surface of the face of a mask user, a respiratory gas conduit means for feeding respiratory gas to a mask internal space which is defined by the arch body and which is in communication with the nose and/or mouth opening of the user of the mask, and an application structure for application of the sealing lip means jointly with the arch body, wherein the application structure has a carrier portion on which a respiratory gas conduit member is releasably coupled.

Abstract: An interface for positive pressure therapy includes a mask assembly, a headgear assembly and a connection port assembly. The mask assembly comprises a seal member that has an upper portion movably connected to an integrated lower portion, wherein the upper portion rolls during hinging movement of the upper portion relative to the lower portion. The headgear assembly allows connection to the mask assembly in a direction substantially normal to a direction of strap tension. The connection port assembly includes a swivel elbow with a valve member that controls flow through a port that opens toward the user.

Abstract: A draining device for draining a fluid line is provided. The draining device comprises a mechanically non-locking coupling and a holding device. The mechanically non-locking coupling is configured to establish a fluid conductive connection with the fluid line. The holding device is configured to stationary fix the mechanically non-locking coupling relatively to the fluid line. The draining device allows establishing a fluid conductive connection between the fluid line and the mechanically non-locking coupling without requiring a mechanical fixation directly at the mechanically non-locking coupling.

Abstract: A mask apparatus for a respiratory treatment can permit delivery of breathable gas to a user. In one example, the mask may employ a frame and cushion to form a seal for both mouth and nose. The frame may be adapted for coupling with a respiratory treatment apparatus so as to permit communication of a pressurized gas from the respiratory treatment apparatus. The cushion, which may be foam, may have a substantially under the nose configuration or over the nose configuration. The mask may have a common plenum chamber for both nose and mouth. The cushion may further define a centrally open lip superior region. The cushion may be adapted to couple with the frame directly or to the frame in conjunction with a cushion support clip. Various features of the cushion may further promote sealing and comfort for the under the nose design.

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: An interface includes a mask. The mask includes a frame and a seal supported by the frame. Headgear is connected to the mask. The interface includes at least one of (i) an adjustment mechanism that can be set to a use length for a loop defined by the mask and the headgear; and (2) a break-fit assembly that can selectively lengthen the loop defined by the mask and the headgear and return to the use length.

Abstract: A connector system includes a catheter connector port to attach to a urinary catheter, a urine exit port to connect to a urine collection device, an irrigation port to receive an irrigation syringe, and an internal valve. The irrigation port includes a pliable membrane that has a self-sealing opening to allow a tip of the syringe to extend therethrough. The internal valve cooperates with the syringe to shut off flow of fluid to the urine exit port when the syringe is inserted and allow for flow of fluid to the urine exit port when the syringe is removed. A distance between a proximal surface of the membrane and a distal end of the internal valve is such that the tip of the syringe can extend from a proximal end of the self-sealing opening to the distal end of the internal valve.

Abstract: Provided is a method, comprising determining, by a processor, a case status corresponding to a power status of a power device of a case and a vaporizer status corresponding to a power status of a power device of a vaporizer device, determining, by the processor, whether power should be transferred between the power device of the case and the power device of the vaporizer device, and causing, by the processor, the determined power to transfer between the power device of the case and the power device of the vaporizer device.

Abstract: Some embodiments of the invention include a tracheal humidification device. The tracheal humidification device may include a first body portion and a second body portion. The first body portion may include a tracheostomy connection port formed to couple with a tracheostomy connection tube; and a heat moisture exchanger port formed to couple with a heat moisture exchanger. The second body portion may be coupled with the first body portion, for example, rotatably coupled. The second body portion may include a nebulizer port formed to couple with a nebulizer and having a closable seal that is closable when the nebulizer is not coupled with the nebulizer port; and a suction port having a closable cap.