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

Abstract: A dry powder inhaler including a housing defining a chamber for receiving a dose of powdered medicament, an inhalation port in fluid communication with the chamber, at least one airflow inlet providing fluid communication between the chamber and an exterior of the housing, and a flutter element in the chamber and associated with a dose of powdered medicament. The flutter element has a tensioned distal end proximate the at least one airflow inlet and a free proximal end opposite to the distal end and downstream of the inlet. The flutter element is configured to vibrate in response to airflow through the chamber and aerosolize the dose of powdered medicament.

Abstract: There is provided a method of determining whether a first type of liquid is being used in a nebulizer, the method comprising obtaining a measurement of the time taken by the nebulizer to nebulize a specified volume of liquid that was held therein, comparing the time taken to nebulize the specified volume of liquid to an estimated value for the time required to nebulize the same volume of the first type of liquid, and determining whether the liquid nebulized by the nebulizer was the first type of liquid based on the comparison.

Abstract: The invention relates to a method and an emergency oxygen supply mask adapted for rescuing a passenger of an aircraft in an emergency situation. In one example, the oxygen mask includes a mask body with a first opening for covering the mouth and/or nose of a passenger and with a second opening connecting the first opening for providing breathable supply air. In some cases, the emergency oxygen supply mask includes a physical reaction component connected to the mask body for receiving air and converting the air into supply air by a physical reaction between the air and a physical reaction material in the physical reaction component to produce oxygen-enriched air. The oxygen-enriched air may be supplied as the supply air to the first opening of the mask body.

Abstract: A patient interface for delivering breathable gas to a patient includes a nasal prong assembly including a pair of nasal prongs structured to sealingly communicate with nasal passages of a patient's nose in use and headgear to maintain the nasal prong assembly in a desired position on the patient's face. The headgear includes side straps and rigidizers provided to respective side straps. Each rigidizer includes a first end portion that provides a connector structured to engage a respective end of the nasal prong assembly and an inwardly curved protrusion in the form of a cheek support that curves inwardly of the connector. The cheek support is adapted to follow the contour of the patient's cheek and guide a respective end portion of the side strap into engagement with the patient's cheek to provide a stable cheek support.

Abstract: A ventilator, or a breathing assistance apparatus, is disclosed to ventilate patients who may have breathing difficulties, said device comprising a inspiratory pressure control duct configured to be immersed in a first body of fluid; a positive end-expiratory pressure control duct configured to be immersed in a second body of fluid; at least one valve connected to the peak inspiratory pressure control duct and to the positive end-expiratory pressure control duct, and at least one controller communicably connected to the valve to control rate of cycling of the valve, thereby controlling number of breaths per minute, and to control the duration of peak inspiratory pressure also known as inspiratory time.

Abstract: A respirator (1) and a mount for a respirator are provided including a mounting device for a cylinder (2), preferably an oxygen cylinder. The mounting device forms an upper housing half (4) and a lower housing half (3) of the respirator (1) and includes at least one grip (6), which makes transportation of the respirator (1) possible. The upper housing half (4) and lower housing half (3) are provided with a connection mechanism (5), which connects the upper housing half (4) and the lower housing half (3).

Abstract: The present invention concerns a plaster for attaching a trachestoma valve or the like in connection with a tracheostoma on a person's neck. The plaster comprises a socket and an annular flange, communicating with a central opening of the flange which is connected with a single-coated adhesive tape which extends radially beyond the edge of the flange. The connection includes a first annular joint at or inwardly of the outer periphery of the flange, and a second annular joint located between the outer periphery of the flange and the inner periphery of the flange spaced radially from the first annular joint. A protecting liner covers the adhesive on the tape.

Abstract: A laryngeal mask airway device inserted in the pharynx of an unconscious patient to ventilate the lungs includes an airway tube and mask portion with cuff formation shaped to fit the actual and potential space surrounding the circumference of the inlet to the larynx. A piriform-fossa conduit is included in a cuff formation of such mask to facilitate insertion of orogastric tubes. Anatomically the piriform-fossa conduit travels around the laryngeal inlet through the piriform fossa to reach the upper esophagus. Structurally the piriform-fossa conduit travels through the lateral cuff formation with the inflatable cuff element. The distal orifice of the piriform-fossa conduit is on the outer perimeter of the cuff formation near the tip of the mask, does not intersect the medial line at the tip, and does not increase bulk in the distal cuff formation along the medial line.

Abstract: A tracheal tube arrangement includes at least one neck strap including, a deformable material. The tracheal tube arrangement further includes at least one reinforcing member integrated into the neck strap. The reinforcing member includes a first opening for receiving a tie. The reinforcing member further includes at least one reinforcement opening for receiving a portion of the deformable material for bonding the reinforcing member to the neck strap. A method of providing a tracheal tube arrangement that has at least one neck strap is also provided.

Abstract: A nebulizer assembly configured for removable attachment to an ultrasonic actuator includes a base plate portion, a porous mesh member, and a cover member. The base plate portion includes an opening extending therethrough, and is substantially rigid such that ultrasonic vibrations from the ultrasonic actuator may be transmitted through the base plate portion to the porous mesh member to vibrate the porous mesh member. The porous mesh member is configured for passage therethrough of a nebulized fluid, and is disposed in the opening of the base plate portion proximate a fluid emission side of the nebulizer assembly. The cover member is disposed on a second side of the nebulizer assembly opposite the fluid emission side. The cover member covers the opening and defines a cavity between the cover member and the porous mesh member. The cavity is configured to retain a fluid to be nebulized.

Abstract: A nozzle unit for discharge of a pharmaceutical medium and a dispenser equipped therewith. The nozzle unit includes a common supply channel for supply of the medium and first and second discharge nozzles each having a discharge orifice for discharge of the medium supplied through the common supply channel. The nozzle unit is configured for atomized delivery of the medium and includes a first vortex chamber assigned to the first discharge nozzle and a second vortex chamber assigned to the second discharge nozzle for the purpose of atomizing.

Abstract: The invention relates to a method of determining water level in a humidifier chamber that is part of a humidified gases delivery apparatus and system. The method comprising the steps of delivering power to a heater plate, varying the power delivered to the heater plate, measuring the rate of change of temperature and determining the level of water based on the heating characteristics of the volume of water within the chamber, in particular determining the level of water within the chamber based on the rate of change of temperature and the supplied power.

Abstract: An improved method for securing a tracheal tube, an adjunct tube, and oropharyngeal tube, a nasogastric tube, a laryngeal tube or laryngeal mask airway to a patient utilizing an elongated strip of adhesive tape, which is specifically adapted therefor.

Abstract: One embodiment is an improved method for providing a tube for attachment to a medical device such as a catheter that provides for intermittent changes in tube path length as a result of body movement thereby reducing the stress and pain caused by pulling on the device, as well as the optional provision to provide a very low, controlled tension that provides improved stability of the medical device without damage to the surrounding body tissues. In at least one embodiment, there is a decrease in infection risk by the patient. This controlled tension can be applied or removed intermittently by a medical practitioner or the patient. Other embodiments provide for extension in tubal path length while simultaneously providing for intermittent or continuous low tension pull on the catheter. Provision is also made for a continuous smooth fluid path with no moving internal parts.

Abstract: A breathing protector for a tracheostoma is provided. The breathing protector comprises an inlet and an outlet, such that an air flow in use will pass from the surroundings of the user through said inlet to said outlet, into trachea of said user. Further, it comprises a filter housing, said filter housing comprising an inner housing part, an outer housing part, and a filter body. The inner housing part, comprising the outlet, a tracheal tube fitting and a support structure extends longitudinally and distally from the tracheal tube fitting. A base plate is arranged in a proximal zone of the tracheal tube fitting, said base plate extending radially outwards from the tracheal tube fitting. The outer housing par, comprising the inlet, forms a cage enclosing the support structure. The filter body is arranged between the support structure and the outer housing part. An assembly tool and an assembly method thereof are also provided.

Abstract: A breathing protector may include an inlet and an outlet, wherein an air flow may be configured to pass from the inlet to the outlet into a trachea. A filter housing may include an inner housing part, an outer housing part, and a filter body. The inner housing party may include the outlet, a tracheal tube fitting and a support structure extending longitudinally and distally from the tracheal tube fitting. A base plate may be arranged in a proximal zone of the tracheal tube fitting and extend radially outwards from the tracheal tube fitting. The outer housing part may include the inlet and form a cage enclosing the support structure. The filter body may be arranged between the support structure and the outer housing part.

Abstract: An inhaler comprising a reservoir of an inhalable composition with an outlet at one end through which the inhalable composition is discharged. A non-metered breath-activated valve is provided between the one end and the reservoir, the breath-activated valve comprising a flow path extending from the reservoir to the outlet end. At least a portion of the flow path is a deformable tube. A clamping member pinches the deformable tube closed when no suction force is applied to the device and releases the tube to open the flow path when suction is applied at the outlet, to provide uninterrupted flow from the reservoir to the outlet.

Abstract: An air warming apparatus operable to provide a user breathing air wherein the air is warmer than that of the user's environment. The air warming apparatus includes a filtered air intake operably coupled to an intake manifold. A lower air transport assembly circumferentially surrounds a user's torso and is adjacent thereto and provides the first phase of air warming for air flowing therethrough. A return manifold operably couples the lower air transport assembly and the upper air transport assembly and further contains a humidifier therein. The upper air transport assembly is surroundably mounted to the user and provides the second phase of air warming. An upper chamber of the intake manifold operably couples the upper air transport assembly and the breathing assembly. The breathing assembly includes a mouthpiece and a breathing valve that is operable to control the air flow through the air warming apparatus.