Abstract: The present application includes an independent and redundant measurement of anesthetic concentration, based on acoustic time-of-flight measurements, added to an anesthetic vaporizer. The redundant anesthetic concentration measurement is used to make the vaporizer inherently safe by design and monitor true vaporizer empty. Further, using an acoustic wave splitting technique and the time-of-flight measurements, the flows at the vaporizer inlet and outlet are computed. The flow measurements are used to monitor carrier gas loss, anesthetic consumption, and anesthetic delivery time remaining and provide such information to the vaporizer operator.

Abstract: According to one aspect of this invention, there is provided a medical facial mask having intubation port to insert an endotracheal tube; air ventilation port to perform artificial ventilation during intubation procedure; and a display device to display image of a patient's airway, wherein the image is transmitted from an image acquisition device which is inserted in the patient's airway.

Abstract: A method and apparatus for automatically controlling partial pressure of oxygen in the breathing loop of a rebreather diving system. A diver may adjustably select a control parameter to maintain partial pressure of oxygen at a setpoint that varies with ambient pressure and is within a range between a maximum safe partial pressure of oxygen at depth and a minimum safe partial pressure of oxygen for the purpose of biasing the performance of the rebreather either towards minimizing gas venting from the rebreather breathing loop or minimizing decompression time. A method and apparatus for managing and monitoring the use of dive resources in comparison with a target dive time specified by the diver, calculating and indicating remaining dive time based on dive resource values and calculating and indicating dive resource values required to meet preselected dive resource end values and dive requirements.

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: A uterine contractile device includes a series of perforated tubes, a sealing balloon, and an additional connecting tube to deliver a vacuum force inside the lumen of a postpartum uterus. The uterine contractile device may be used after child birth to facilitate contraction of a woman's uterus. By facilitating contraction of the uterus, a medical professional may achieve immediate and sustained hemostasis of the mother.

Abstract: An active inhaler for delivery of an inhalation formulation has an overall flow resistance of at least 60,000 Pa1/2 s/m3 for ambient air drawn into a mouthpiece of the inhaler. This flow resistance when air and the aerosol are sucked via the mouthpiece is produced by the sizing of at least on air supply opening and/or an insert within the mouthpiece.

Abstract: The present invention describes a medical, supply or transfer lock (120) for a pressure vessel (100) for human occupancy. The medical lock (120) includes a body tube (122), an outer door flange (124) and an outer door (140) in sealing face relation with an inside face (125) of the outer door flange (124). In an embodiment, the outer door (124) has upper rollers (146a) and lower rollers (146b). The upper rollers run on a horizontal rail (160) while the lower rollers run on a slant rail (170), which is mounted below the horizontal rail (160). The ends of the horizontal and slant rails (160,170) are curved (163, 172) so that weight component of the outer door is generated to assist the outer door to close. When pressure in the medical lock (120) is increased, the outer door (140) of this medical lock (120) becomes self-locking and self-sealing.

Abstract: A bio-compatible lumen bearing device such as a catheter formed of a polymeric material having a titanium surface bonded to the underlying exposed catheter surface. The titanium surface is employed in patients to improve bio-compatibility and enhance lubricity during insertion and removal.

Abstract: Systems and methods are presented for providing reduced pressure to and monitoring pressure at a plurality of tissue sites using a plurality of pressure management devices. The pressure management devices are associated with a plurality of sensing conduits that fluidly couple the pressure management devices and the plurality of tissue sites. Other systems, methods, and devices are disclosed.

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 and controlling the pressure in the inflatable cuff (26) is described, which, in one embodiment, controls the pressure about a setpoint pressure, whilst preventing loss of sealing pressure during a patient's respiratory cycle. In other embodiments, the method and apparatus monitors for: 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: An indicator arrangement for a regulator removably connectable to a facemask in a breathing apparatus, the indicator arrangement including: at least one release button comprising a body operationally engaged with at least one component of the regulator and configured to be actuated by a user to detach the regulator from the facemask, wherein at least a portion of the body is configured to facilitate transmission of light from at least one light source; and wherein the light is visible on or through at least one external surface of the body of the at least one release button. A regulator release button and breathing apparatus are also disclosed.

Abstract: The disclosure relates to a medical dispenser, comprising an outlet and a plurality of sealed compartments containing medicament to be sequentially aligned with and dispensed through said outlet. Movement of an actuator sequentially causes mechanical energy to be built up and then released and converted into an indexing movement of the compartments. The disclosure also relates to an indexing method for a medical dispenser.

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 and controlling the pressure in the inflatable cuff (26) is described, which, in one embodiment, controls the pressure about a setpoint pressure, while preventing loss of sealing pressure during a patient's respiratory cycle. In other embodiments, the method and apparatus monitors for: 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 two piece ostomy appliance having a first part (bodyside part) adapted for securing to the body of a user, and second part (pouch part) that is releaseably secured to the first part. The pouch part has a pouch flange which has an opening communicating with an interior of the pouch; and a bodyside flange with an opening and a hydrocolloid layer for securing the bodyside flange to the stoma of a user. The bodyside flange has a location projection receivable in a recess in a part of the pouch flange to align the opening of the pouch flange with the opening of the bodyside flange. A surface of the pouch flange has an adhesive to adhere the pouch flange to the bodyside flange. The recess of the pouch flange is located at the periphery of the pouch flange, extending away from the opening in the pouch flange.

Abstract: The present invention concerns a tracheostomy cannula comprising a cannula tube, wherein the cannula tube has a bend with a radially inward and a radially outward side of the cannula tube and a tube lumen and a tube wall and an axis extending parallel to the tube wall in the tube lumen and a distal and a proximal end and on the radially outward side of the bend a first window region having one or more openings in the tube wall. To provide a tracheostomy cannula having a cannula tube, with which talking is made possible and the entry of air into the tissue is prevented even when the position of the tracheostomy cannula in the trachea or the anatomical conditions change, it is proposed in accordance with the invention that the cannula tube has in axially displaced relationship with the first window region at least one further window region having one or more openings in the tube wall.

Abstract: An inhaler which comprises a base having a plurality of consecutive sealed cavities containing medicament. Foil portions are on one side attached to the base for sealing the medicament within respective associated cavities. A plurality of separating elements are attached to the other side of the foil portions, each separating element being associated with a respective cavity for separating a foil portion from that cavity. Each separating element can be moved-away from its associated cavity so that the sealing foil portion is separated from the cavity which is thereby uncovered so that medicament contained therein is enabled to become entrained in a fluid flow, and then returned with the attached foil portion to cover its associated cavity. A method of operating an inhaler is also disclosed.

Abstract: An embodiment of a uterine hemorrhage controlling system comprises a suction module including a suction end coupleable to a pump by a connecting tube, and a sealing module coupled to the suction module. The system may further comprise the pump and a filter coupled to the suction module. A uterine hemorrhage controlling method comprises: shielding a suction module that has been delivered into a uterus; sealing an entrance into the uterus while the suction module is situated within the uterus; applying a negative pressure within the uterus upon activation of a pump; and maintaining the negative pressure within the uterus to induce uterine contraction. The method may further comprise delivering the suction module into the uterus; transmitting bodily fluids, out of the uterus through the suction module, and filtering the bodily fluids.

Abstract: A fluid dispenser device including a body, a dispenser mechanism, and a dose counter. The counter includes a first rotary counter element provided with a first surface including a first indicator, such as digits, and provided with at least one first set of teeth, a second rotary counter element provided with a second surface including a second indicator, such as digits, and provided with at least one second set of teeth, and a movable actuator element. The first counter element includes at least one deformable finger displaceable between a non-deformed position and a deformed position, and that is adapted to co-operate, in its deformed position, with the second set of teeth of the second counter element, so as to cause the second counter element to turn. The body includes a cam that is adapted to deform the deformable finger towards its deformed position.

Abstract: The prevention invention relates to a moxa holder support and a moxibustion device comprising the same, and more particularly, to a moxa holder support which provides comfort to a patient receiving moxibustion, and to a moxibustion device in which the temperature of part of a human body, to which moxibustion is applied, can be easily controlled according to the characteristics of the related organ of the human body. When receiving moxibustion using the moxa holder support according to the present invention, a patient can feel comfortable because part of the patient's skin to which moxibustion is applied comes into contact with the leather connected to the bottom of a main body of the moxa holder support and the texture of pig skin, cow skin or sheep skin used as the leather in the present invention is similar to that of human skin.

Abstract: A delivery device for delivering a metered amount of substance, the delivery device comprising: a mouthpiece (17) through which a user in use exhales; an outlet (19) through which substance is in use delivered; a housing (21) fluidly connected to the mouthpiece and the outlet, such, that exhalation by the user through the mouthpiece creates an air flow through the housing and from the outlet; and a substance-dispensing unit (25) which is disposed within the housing and operative to dispense a metered amount of substance into an entraining air flow as created through the housing.