Abstract: Disclosed is a transtracheal ventilation device including at least one base plate with an opening and comprising a tubular connecting part with a channel and a central axis. The base plate and the connecting part are connected to each other such that a lumen, when inserted into the device, extends into the channel through the opening along the central axis to a fixing element (a fastening). The fixing element can be pivoted relative to the central axis. The fixing element is arranged at a distance of at least 5 millimeters along the central axis from a base plate face which faces away from the fixing element, and the opening has an inner diameter which is at least 20% larger than an outer diameter of the lumen at least on a first plane perpendicular to the central axis.

Abstract: The volume of a pressure equalization balloon is connected to a further volume, the pressure of which is intended to remain as constant as possible. To keep the cuff pressure in the pressure range of between roughly 20 mbar and 30 mbar, the equalization balloon is produced from a thermoplastic polymer (TPE) and is overstretched past the maximum intended control volume before first use and is then relaxed to the range of the control volume.

Abstract: A component (10) of a respiratory apparatus is disclosed, which comprises a gas passageway defined by an enclosing wall (20,30), and a port (40) in the enclosing wall (20,30) adapted to receive an ancillary device (60). The component (10) also includes a retaining arm (50) that is movable between an open configuration in which an ancillary device (60) may be engaged with the port (40), and a retention configuration in which the retaining arm (50) acts, in use, to resist removal of the ancillary device (60) from the port (40).

Abstract: Provided is an endotracheal tube, which comprises a baffle, an endotracheal tube body and a pharyngeal suction catheter and is integrally formed. The pharyngeal suction catheter is fixedly connected with an outer wall of the endotracheal tube body. One end of the pharyngeal suction catheter is bent to form a front bent portion, a port of the front bent portion is closed and a side wall of the front bent portion is provided with two suction ports. In the case of oral endotracheal intubation, the pharyngeal suction catheter is introduced to the bottom of the pharynx as the endotracheal tube body is inserted into the weasand, and the pharyngeal suction catheter can stay there for a long period of time, enabling high efficiency of removal of pharyngeal secretions, the reduction of discomfort and adsorption injury of the patient, and the reduction of nursing workload.

Abstract: The invention relates to a speaking valve for laryngectomized and tracheotomized persons that is easy and economical to produce. According to the invention, the speaking valve comprises a proximal first opening and a distal second opening, a filter, which is at least partially surrounded by the housing, which filter is made of an elastic material, and has a proximal first end and a distal second end, wherein the filter partially protrudes beyond an end face of the housing at the distal second opening, and wherein a cover is connected by means of at least one partial region of the bottom surface thereof to a top side of the filter at the distal second end of the filter.

Abstract: A tracheal/endotracheal device that has an integrated system for removing mucins and similar infectious secretions. The tracheal/endotracheal device has several channels. One channel delivers air to a patient's lungs. At least two other channels cooperate to deliver a mist of antiseptic ingredients to an area in the trachea and to suction away the mist and any mucins and secretions. The mist and bodily fluids captured by the suctioning channel are delivered to a collection vessel outside of the trachea.

Abstract: Intubation devices, systems, and methods in which the risk of leakage of nasopharyngeal secretions, esophageal reflux, and blood is reduced, or eliminated, by means of a backflow pressure gradient that is independent of PEEP. Contemplated configurations include (a) a flexible tube for the controlled delivery of air and other gases to the lungs, (b) distal and proximal inflatable seals that can close the annular space surrounding the tube, (c) means to inflate the seals, and (d) means to deliver gas under pressure to the annular chamber in between the two seals. Further configurations further comprise a processor and sensors, and methods are provided for automated backflow of contaminated fluids.

Abstract: The present invention relates to a novel tracheal cannula (10), which allows patients to speak who receive artificial respiration with compressed-air. The tracheal cannula according to the invention makes this possible without the risk that saliva or stomach content is aspirated and without the occurrence of a loss of pressure during the respiration. This is achieved by an embodiment of the cannula having a separated speaking conduit (12) and respiration conduit (11). Furthermore, the invention relates to a speaking respiration system that can be connected to the tracheal cannula of the present invention, and that when used in a patient monitors and controls the respiration of the patient, and simulates an artificial exhalation that enables the tracheostomized patient to speak.

Abstract: A laryngeal mask for use in a patient includes an airway tube having an inner lumen and a distal end; and a mask portion connected at a proximal end thereof to the distal end of the airway tube and having a distal tip opposite the proximal end. The mask portion includes an inflatable cuff including an anterior cuff surface configured to contact the patient's tissue when the inflatable cuff is inflated; and a wedge portion including a stabilization surface and two walls connected to the inflatable cuff and extending therefrom toward the stabilization surface, the stabilization surface extending from the distal tip of the mask portion toward the distal end of the airway tube at a wedge angle of between about 12 and 30 degrees, the wedge angle formed between the stabilization surface and the anterior cuff surface when the inflatable mask is inflated, whereby the stabilization surface is transversely and longitudinally substantially flat to stabilize the laryngeal mask in use.

Abstract: An airway device (14), that is used to maintain a clear airway in a patient, e.g. for artificial ventilation during surgery, comprises an inflatable cuff (26), which is inflated when in position in a patient's airway (24). The inflated cuff (26) provides a seal to maintain the device (14) in position in a patient's airway (24), and to prevent leakage of infected oropharangeal secretions into the patient's lungs. A method and apparatus (10) for monitoring: leaks in the pressure system of the device (14) that includes the cuff (26); blockage in the pressure system, and/or malpositioning of the airway device (14) during use.

Abstract: A laryngeal mask for use in a patient includes an airway tube having an inner lumen and a distal end; and a mask portion connected at a proximal end thereof to the distal end of the airway tube and having a distal tip opposite the proximal end. The mask portion includes an inflatable cuff including an anterior cuff surface configured to contact the patient's tissue when the inflatable cuff is inflated; and a wedge portion including a stabilization surface and two walls connected to the inflatable cuff and extending therefrom toward the stabilization surface, the stabilization surface extending from the distal tip of the mask portion toward the distal end of the airway tube at a wedge angle of between about 12 and 30 degrees, the wedge angle formed between the stabilization surface and the anterior cuff surface when the inflatable mask is inflated, whereby the stabilization surface is transversely and longitudinally substantially flat to stabilize the laryngeal mask in use.

Abstract: A catheter assembly incorporating a pre-biased indicator, the assembly includes a catheter having a proximal end, a distal end, and catheter walls defining a catheter lumen. The assembly further includes a base located at the proximal end of the catheter, the base defining an opening to the catheter lumen, the base having a first end and a second end. An inflatable balloon having a predetermined fill volume is located at a distal end of the catheter. An inflation valve is located on the base; the inflation valve is in fluid communication with the balloon through an inflation lumen defined by the catheter walls. The pre-biased indicator located on the base in fluid communication with the balloon is configured to provide a discrete visual signal that the pressure of a fluid in the balloon is different from a predetermined level of pressure or the volume of the balloon is different from the predetermined fill volume.

Abstract: Techniques for single lung ventilation (SLV) include a hollow main tube with outer diameter sized to fit inside a bronchus of a patient. The length of the main tube is sufficient for a distal end of the main tube to reach a first side bronchus from a proximal end configured to be located in a vicinity of a mouth of the patient. The hollow main tube has a ventilating orifice separated from the distal end at a location that corresponds to a different second side bronchus. A hollow tubular sleeve is moveably disposed inside and longitudinally aligned with the main tube. The sleeve is configured to be positioned in at least two positions: a first position that does not block the ventilating orifice; and, a second position that does block the ventilating orifice.

Abstract: An implantable device for releasing one or more substances into a body cavity such as a urinary bladder, is provided. The device includes an inner balloon located within an outer balloon so as to define a lumen between the outer and inner balloons. A first valve is used for filling the lumen; and a second valve is used for filling the inner balloon. The device is delivered to the body using a delivery catheter. The inner portion is filled with the substance or substances to be released into the body cavity. The outer balloon is filled with a substance that is chosen to impart a desired specific gravity to the device. The substances to be released may be contained in particles coated with a soluble coating. The particles may be in suspension or embedded in a matrix.

Abstract: An airway device for use with deep sedation has a pair of conduits, one to supply oxygenated gas and the other to extract exhaled gas. The conduits are encompassed in a permeable sleeve with a stylet to facilitate positioning of the device in the airway.

Abstract: The disclosed subject matter describes systems and methods of delivering a therapeutic agent, such as a sclerosing agent, to the walls of a blood vessel to perform sclerotherapy. In an exemplary embodiment a catheter includes a guidewire catheter having at least one guidewire lumen extending therethrough and a slidable concentric tube disposed over the guidewire catheter. At least one bellow is coupled to the concentric tube and configured for conversion between an unexpanded and expanded configuration wherein movement of the concentric tube in a first direction causes the at least one bellow to expand and movement of the concentric tube in a second direction causes the at least one bellow to contract. Additionally, the concentric tube contains at least one port for delivery of a therapeutic agent, e.g. a sclerosing agent. The at least one bellow expands and contracts via mechanical forces.

Abstract: The present invention provides an improved means of treating tracheobronchitis, bronchiectasis and pneumonia in the nosocomial patient, preferably with aerosolized anti gram-positive and anti-gram negative antibiotics administered in combination or in seriatim in reliably sufficient amounts for therapeutic effect. In one aspect, the invention assures this result when aerosol is delivered into the ventilator circuit. In one embodiment the result is achieved mechanically. In another embodiment, the result is achieved by aerosol formulation. In another aspect, the invention assures the result when aerosol is delivered directly to the airways distal of the ventilator circuit. The treatment means eliminates the dosage variability that ventilator systems engender when aerosols are introduced via the ventilator circuit.

Abstract: This invention relates generally to a diagnostic and therapeutic device. According to some aspects of the invention, the device may be composed of a flexible sheet that is wrapped around the endoscope shaft to form a flexible overtube. The overtube may include an inflatable positioning ring that may be inflated after placement of the overtube just proximal to the tip of the endoscope or colonoscope to secure the position of the overtube within the body cavity. The overtube also may include an inflatable sealing band within the internal surface of the overtube that when inflated create a seal around the endoscope shaft. According to other aspects of the invention, the device may be a catheter with an occlusion balloon at its free end portion that is carried by the overtube and extends beyond the tip of the endoscope. Inflation of the positioning ring, sealing band and occlusion balloon may define an examination compartment within the body cavity at the tip of the endoscope.

Abstract: Medical devices and methods of treatment are described herein. More particularly, medical devices and methods for providing access to a bodily passage during dilation are described herein. An exemplary medical device comprises an elongate member and a balloon. The elongate member is moveable between a first, non-expanded configuration and a second, expanded configuration.

Abstract: A urinary catheter may include a catheter shaft and a connector coupled with the proximal end of the catheter shaft. The connector may have a first arm ending in a fluid outlet configured to allow urine to flow out of the urinary catheter and a second arm with an aperture and ending in an inflation inlet used for introducing inflation fluid into the urinary catheter. The catheter may further include a primary lumen, an inflation lumen, a retention balloon mounted to the catheter shaft proximal to a fluid inlet and over a distal filling hole, and a pilot balloon mounted on the second arm of the connector over the aperture. The pilot balloon inflates at an inflation pressure that is higher than the inflation pressure of the retention balloon and lower than a predetermined pressure threshold.

Abstract: The present invention provides a method and apparatus for treating a vascular occlusion and preventing or reducing ischemic consequences of such an obstruction. The medical device of the present invention may include an elongate body defining a proximal end and a distal end, where the elongate body may also define an injection lumen, an exhaust lumen, and a guidewire lumen. A first expandable element may be coupled to the elongate body, where the first expandable element is in fluid communication with the injection lumen and the exhaust lumen. Further, a perfusion path may be disposed within the elongate body, and a sheath may be movably disposed about at least a portion of the elongate body. The medical device may further include a second expandable element disposed about the elongate body, as well as second inflation and exhaust lumens.

Abstract: Penetrating systems and devices are described herein which include a penetrating portion having a fluid reservoir portion formed from two concentric hollow cylinders joined at one end with a substantially ring-shaped first end piece and associated at the other end with a substantially ring-shaped second end piece, the outer hollow cylinder including a plurality of pores in fluid communication with the fluid reservoir portion, the inner hollow cylinder defining a lumen in fluid communication with a second fluid reservoir portion, and the substantially ring-shaped second end piece forming a deformable barrier.

Abstract: A scaffold strut is shaped to improve hemocompatibility. The scaffold is made from a tube having variable wall thickness. Methods are disclosed for modifying the thickness of the tube in such a way as to achieve a reduced hemodynamic profile, but without significantly affecting strength properties in areas where stress concentrations exist when the scaffold is loaded.

Abstract: Various embodiments of a tracheal tube capable of suctioning accumulated mucus secretions from the airway of intubated patients are provided. Disclosed embodiments include a variety of endotracheal tubes with integral suction lumens terminating in ports optimally located at the distal end of the endotracheal tubes between a Murphy's Eye and a cuff. During intubation, the foregoing features, among others, of the tracheal tube may have the effect of preventing bacterial colonization of the respiratory airway and the subsequent development of ventilator associated pneumonia (VAP) in the lungs.

Abstract: A laryngeal mask includes an airway tube having an inner lumen and a distal end; and a mask portion connected at a proximal end thereof to the distal end of the airway tube and having a distal tip opposite the proximal end. The mask portion includes an inflatable cuff including an anterior cuff surface, and a wedge portion including a stabilization surface and two walls connected to the inflatable cuff and extending toward from the stabilization surface, the stabilization surface extending from the distal tip of the mask portion toward the distal end of the airway tube at a wedge angle of between about 12 and 30 degrees, the wedge angle formed between the stabilization surface and the anterior cuff surface when the inflatable mask is inflated. The stabilization surface is transversely and longitudinally substantially flat to stabilize the laryngeal mask in use.

Abstract: The present disclosure describes an endotracheal tube for a child, the tube having a balloon mounted near the distal end of the tube. The tube has a ventilation lumen and an inflation line used to inflate the balloon. The balloon is mounted to the tube at a lower mounting point and an upper mounting point. The upper mounting point is above the level of the vocal cords. The balloon has a lower and upper diameter when inflated, and the upper diameter is from 1.1 to 1.5 times larger than the outer diameter of the tube.

Abstract: A naso/orogastric device that comprises a naso/orogastric tube sized and shaped for being disposed within the esophagus so that at least a distal segment thereof being placed in the stomach lumen of a patient and at least one self expending element disposed around a peripheral surface of the naso/orogastric tube and having a first thickness in a compressed state and a second thickness in an expanded state, the at least one self expending element switching from the compressed state to the expanded state when absorbing moisture. The first thickness is thinner than the second thickness.

Abstract: An airway stabilization system attachable to any airway device to maintain an airway in a patient and which prevents clinically significant movement of the airway device with respect to the patient's vocal cords in response to the application of significant forces in any direction to the device, be they longitudinal, torsional/rotational or bending. The system includes an improved airway device and an improved securing device having interactive components that cooperate integrally with and engage one another to provide unparalleled strength and stability against movement. The securing device includes a unique stabilizer configured to releaseably engage a retention structure on the airway device with a simple twist. A connector device connects the system to a source of ventilatory air without constricting the airway device.

Abstract: In various embodiments, a device is provided comprising a balloon configured to expand to an expanded state in response to introduction of a fluid at a first pressure, wherein the fluid perfuses through the balloon above a second pressure, the second pressure being the same or greater than the first pressure. In various embodiments, a method comprising fabricating a balloon configured to expand to an expanded state in response to introduction of a fluid at a first pressure, wherein the fluid perfuses through the balloon above a second pressure, the second pressure being at or greater than the first pressure, disposing the balloon on an elongate member having a lumen, placing the lumen in fluid communication with an interior volume of the balloon.

Abstract: Various embodiments of an intubation system include a tracheal tube and an illumination assembly that is removably couplable to a tubular body of the tracheal tube. The tracheal tube may be a double lumen tracheal tube having a first cuff that is adapted to be inflated to seal against the walls of a patient's trachea and a second cuff that is adapted to be inflated to seal against the walls of the patient's bronchial stem. The illumination assembly may have one or more illumination devices that are adapted to produce light within the patient's trachea, the patient's bronchial stem, or both when the illumination assembly is coupled to the tubular body.

Abstract: Described here are devices and methods for measuring a distance in an airway. In some instances, the devices may comprise an outer shaft and an inner shaft that is slidably disposed in a lumen of the outer shaft. An expandable stopper may be positioned at a distal end of the inner shaft, which may be configured to engage a carina of a patient. The device may comprise one or more alignment markings and one or more displacement markings that may be used to measure a distance between a distal tip of an endotracheal tube and the carina. In some variations, measurement may be facilitated by the use of an alignment guide that may attach to a predetermined portion of an endotracheal tube.

Abstract: A device for maintaining an airway in a patient, the device including a mask having a peripheral portion that forms a seal with the larynx when the mask is positioned in the laryngo pharynx to thereby prevent ingress of extraneous fluids into the larynx; an airway tube connected to or formed with the mask for passing gas to the larynx when the mask is properly inserted into the laryngo pharynx; and one or more elongated members located on the mask, wherein the application of force to the elongated members causes elastic deformation of the device, thereby facilitating insertion of the device into the patient.

Abstract: Angioplasty or valvuloplasty balloon catheters with a ripcord for cutting, ripping, or tearing a balloon can achieve faster deflation times. Methods using such catheters can improve patient outcomes in percutaneous transluminal valvuloplasty and angioplasty.

Abstract: A laryngeal-mask airway device including provision for drainage of the esophagus including an inflatable main-cuff and a backplate having a laryngeal-side and a pharyngeal-side. The backplate also has an external tube joint adjacent to the proximal region of the main-cuff. The backplate is hermetically bonded to the periphery of the main-cuff establishing separation between a laryngeal-chamber region and a pharyngeal region. A distally open evacuation tube includes a distal portion which longitudinally traverses the interior of the distal region of the main-cuff in sealed relation therewith for operative engagement and communication with the inlet of the oesophagus. The evacuation tube traverses the laryngeal-chamber region generally adjacent to the laryngeal-side of the backplate and passages through a proximally located tube-joint to the pharyngeal region.

Abstract: A medical apparatus having a nasogastric tube with hypopharyngeal suctioning capability. In one embodiment, the medical apparatus has a flexible nasogastric tube for insertion through a patient's nose. The nasogastric tube has a first end defining a first opening, a distal, second end that defines a second opening, and a length sufficient to allow the second opening to be positioned in a patient's stomach. The medical apparatus also has a flexible oropharyngeal tube for insertion through a patient's mouth. The oropharyngeal tube has a first end defining a first opening and a distal, second end that defines a suction intake. The oropharyngeal tube has a length that is less than the length of the nasogastric tube and which allows the suction intake to be positioned in a patient's hypopharynx region.

Abstract: An artificial airway device to facilitate lung ventilation of a patient, having an airway tube, a gastric drain tube and a mask at one end of the airway tube, the mask including a backplate and having a peripheral formation capable of forming a seal around the circumference of the laryngeal inlet, the peripheral formation surrounding a hollow interior space or lumen of the mask and the airway tube opening into the lumen of the mask, wherein the mask includes an atrium for passage to the gastric drain tube of gastric matter leaving the esophagus is disclosed.

Abstract: A surgical instrument configured for insertion through a surgical access device including a seal member is disclosed. The surgical instrument includes an elongate body having a central passageway extending at least partially therethrough and a plurality of slots extending radially outward from the central passageway. The plurality of slots are configured to engage the seal member and the surgical access device when the elongate body is translated therethrough to remove debris from the seal member and the surgical access device. The plurality of slots and the central passageway are configured to retain the removed debris therein during withdrawal of the surgical instrument from the surgical access device.

Abstract: A treatment device includes: a balloon; a biologically active agent part applied on an outer surface of the balloon; a protective sleeve encircling the balloon and being displaceable proximally; and an interposed member having a self-expanding function arranged between the balloon and the protective sleeve. When the protective sleeve is moved proximally in order for the balloon to be exposed to the inside of a blood vessel, the presence of the interposed member prevents the biologically active agent part from being scraped and peeled off by the inner surface of the protective sleeve.

Abstract: An airway manifold includes a manifold body having an upper body portion and a lower body portion. The body portions are engaged such that the upper body portion is rotatable relative to the lower body portion, whereby a generally hollow interior space is defined. The lower body portion has a port open to the interior space, and the upper body portion includes a plurality of ports open to the interior space. A first upper body port is axially alignable with the lower body port to define a substantially linear passageway therebetween when the upper body portion is at a first rotatable position relative to the lower body portion. A second upper body port is axially alignable with the lower body port to define a substantially linear passageway therebetween when the upper body portion is at a second rotatable position.

Abstract: A respiratory interface device (10, 20, 30, 40, 50, 60, 70, 80) comprising a main body (12, 22, 32, 42, 52, 62, 72, 82) that includes a fluid conduit adapted to be connected to a breathing circuit, and a sealing member (15, 25, 35, 45, 55, 65, 75, 85) adapted to engage a surface of a patient, such that the fluid conduit is in fluid communication, in use, with an airway of the patient, wherein the sealing member (15, 25, 35, 45, 55, 65, 75, 85) includes a plasticizing agent, and a barrier member (18, 28, 38, 48, 58, 68, 78, 88) is provided between the sealing member (15, 25, 35, 45, 55, 65, 75, 85) and the main body (12, 22, 32, 42, 52, 62, 72, 82) of the device (10, 20, 30, 40, 50, 60, 70, 80), the barrier member (18, 28, 38, 48, 58, 68, 78, 88) at least impeding the migration of plasticizing agent from the sealing member (15, 25, 35, 45, 55, 65, 75, 85) to the main body (12, 22, 32, 42, 52, 62, 72, 82) of the device (10, 20, 30, 40, 50, 60, 70, 80).

Abstract: A system for treating uterine tissue having a seal assembly configured for positioning in a patient's cervical canal and uterine cavity; an expandable distal balloon portion; an expandable elongate medial balloon portion configured for movement between a first transversely expanded shape for engaging a cervical canal and a second transversely non-expanded shape for trans-cervical insertion; and a fluid source in communication with distal balloon portion and medial balloon portion for expansion of said balloon portions.

Abstract: In an embodiment, a tracheal tube system has a first tube, which is flexible. The tube has an opening that is located on the sidewalls. A balloon is attached to the flexible tube. When inflated, the balloon forms a second tube surrounding the first tube with an air space between the first wall of the balloon and the sidewalls of the first tube. The balloon extends covering the opening on the sidewall. Air flowing into the first tube exits, via the third opening into the airspace between the first tube and the balloon, out of the airspace. In another embodiment, the balloon has a tube with multiplicity of holes in the walls is wrapped around the outer wall of the balloon. Negative pressure in the third tube creates suction holding the outer wall of the balloon to walls of the trachea.

Abstract: An inflatable balloon for diagnostics and treatment of diseased discs or fractured bones. The balloon is a multi-volume balloon comprised of a plurality of adjustable and expandable single volumes. Further disclosed are methods of forming, expanding, and implanting the multi-volume balloon for proper placement and stabilization of the diseased discs or fractured bones. Still further disclosed are kits for aligning and stabilizing a bone, disc, or spinal motion segment.

Abstract: An endotracheal tube for mechanically ventilating patients is disclosed. The endotracheal tube comprises a distal end for insertion into the patient's airway, past the vocal chords, through the subglottal region, and into the patient's lung; and a proximal end for connection to a mechanical ventilator. The endotracheal tube further comprises a cuff at the distal end of the endotracheal tube to be located in the subglottal region of the patient below the vocal chords, an inflating lumen for inflating the cuff, and a suction lumen having a suction inlet port leading from the outer surface of the endotracheal tube, and to be located in the subglottal region, for evacuating secretions and/or rinsing fluid from the subglottal region during the mechanical ventilation of the patient.

Abstract: Devices and methods for preventing tracheal aspiration as described where a cuff assembly having an inflatable member with an inflation tube fluidly coupled may be placed over a proximal end of an endotracheal tube or laryngeal mask and inserted into the patient trachea with the endotracheal tube or separately after the endotracheal tube has already been positioned. In either case, the inflatable member may be positioned distal (or inferior) to the vocal cords and proximal to the endotracheal balloon via a delivery instrument which automatically positions the balloon in proximity to the vocal cords.

Abstract: This invention relates generally to an endoscope accessory. This device uses an overtube with an inflatable positioning ring that can be inflated after placement of the overtube just proximal to the tip of the endoscope or echoendoscope. A catheter with an occlusion balloon at its free endportion is carried by the overtube and extends beyond the tip of the endoscope, distal to the part of the body cavity that needs to be examined. Inflation of this balloon together with positioning ring creates a closed space within the body cavity that can be filled with air or water for improving the quality of the examination with regular endoscope of echoendoscope, respectively, while reducing the examination complications.

Abstract: A fluid pressure indicating device is disclosed. The pressure indicating device includes a housing defining a cylindrical bore therein, and a piston movably disposed within the cylindrical bore. The housing includes a first portion that is permeable to visible light, a first end member, and a second end member opposite the first end member. A first variable volume is defined by the cylindrical bore, the piston, and the first end member of the housing. An inlet port is defined by the first end member of the housing and is in fluid communication with the first variable volume. A piston bypass channel is disposed outside the cylindrical bore and is in fluid communication with the inlet port. An outlet port is defined by the second end member, such that the outlet port is in fluid communication with the piston bypass channel.

Abstract: A tracheal tube assembly includes an outer cannula configured to be positioned in a patient airway and an inner cannula configured to be disposed inside the outer cannula. The tracheal tube assembly further includes a flange member secured about the outer cannula, and a connector coupled to a proximal end of the outer cannula. The connector is configured to provide a view of the inner cannula, and the inner cannula and the connector form a contiguous passageway for exchanging fluid with the patient airway in operation.

Abstract: The present disclosure relates to a leak detection system and method for tube or catheter placement. The system and method includes acoustically sensing a leak in the seal between a tube or catheter within a body and the body cavity against which it is sealed, assisting the user in adjusting the system until the leak has been substantially sealed, and establishing system parameters to be used thereafter to maintain the system in an operating state that will substantially prevent leakage, all using a noninvasive acoustic technique.

Abstract: The invention relates to a laryngeal mask airway device to facilitate lung ventilation in a patient, comprising an airway tube extending from a proximal end to a distal end and opening, at the distal end, into the interior of a hollow mask portion shaped to fit readily in use into the actual and potential space behind the larynx and to seal around the circumference of the laryngeal inlet without penetrating into the interior of the larynx, wherein the device comprises a conduit adapted to direct a liquid substance through the glottic opening. The invention further relates to a kit comprising the laryngeal mask airway device and a method for using the laryngeal mask airway device.