An airway management device has a body (6) including an external shell moulded from a polypropylene copolymer (PP) blended with a thermoplastic elastomer (TPE) of styrene-ethylene/butylene-styrene (SEBS), the external shell extending from a proximal opening to a distal tip of the body (6), the external shell having a curved portion (35) and a linear portion (37). Methods of manufacturing are also disclosed.

A nasal cannula assembly is disclosed having a face mount part, in use resting against a user's face, which includes at least one nasal prong capable of being fitted into a person's nares. The cannula assembly also includes a manifold part, in fluid communication with the face mount part, having a single horizontal side gases entry. In particular, this cannula assembly is for supplying heated, humidified gases to a patient suffering from COPD. A tie or lanyard is disclosed for use with a breathing assistance apparatus such as a nasal cannula, face or nasal mask or tracheostomy connector. The tie or lanyard transfers the weight of the conduits supplying gases to the breathing assistance apparatus from the breathing assistance apparatus and distributes it onto the neck of the patient.

The present disclosure relates to airway devices. It is applicable to supraglottic devices including laryngeal airway devices and to their methods of manufacture. The present disclosure is particularly applicable to laryngeal airway devices for human and veterinary use. The device includes an airway tube having a distal end and a proximal end, the distal end of the airway tube is provided with a pre-formed and non-inflatable peri-pharyngeal bowl. The peri-pharyngeal bowl includes a posterior bowl portion having a back dorsal portion and a side wall extending around and depending from the periphery of the back dorsal portion to define an internal space, and further includes a resiliently deformable flange extending laterally from the side wall of the back dorsal portion which defines an extended internal space, the resiliently deformable flange has inner and outer surfaces that extend to a circumferential edge.

A dual suction tube is provided that includes a lower section, an upper section, and a transitional zone. The lower section includes at least one eyelet disposed at a distal end of the lower section. The upper section includes at least one port configured to be connected to a vacuum source. The transitional zone is between the lower section and the upper section, and has a first cross-sectional area at a proximal end of the transitional zone and a second cross-sectional area at a distal end of the transitional zone. The first cross-sectional area is greater than the second cross-sectional area.

An airway management device comprising a body having a proximal end for receiving an oxygen supply tube and an distal end for insertion into a trachea of a patient; said body including a linear portion adjacent to the proximal end and a curved portion adjacent to the distal end; said body including an external shell and having a first bore through said shell for receiving the oxygen supply tube; wherein flexural strength for said airway management device is provided by said shell.

The present invention provides an inflatable laryngeal mask airway (LMA) for endoscopic diagnosis and treatment. The inflatable LMA for endoscopic diagnosis and treatment includes a cuff and an airway tube. The cuff is fixedly connected to the airway tube. The airway tube includes a ventilation airway, an endoscope channel and an inflation channel which are arranged in parallel. The ventilation inlet, the endoscope inlet and the inflation inlet are located at the end of the airway tube away from the cuff. The cuff includes a base body and an air bag connected to the base body. The inflation outlet is connected to the air bag. The endoscope outlet is connected to a lower surface of the base body and directed to the front side of the base body. The back surface of the endoscope channel is provided with an expansion port extending from the endoscope inlet to the endoscope outlet.

A pharyngeal tube for establishing an airway within a patient may comprise an elongated hollow tube including a proximal end and a distal end. A mouthpiece may be provided at the proximal end of the tube, and one or more lateral openings may be provided at or near the distal end of the hollow tube. The one or more lateral openings may be formed in a lateral wall of the hollow tube, and a distal tip of the hollow tube is sealed so that air cannot escape the tube from its distal tip. The mouthpiece may form an airtight seal at the patients mouth. The mouthpiece may include an inner flange configured to be positioned between the patients teeth and lips, and an outer flange configured to be positioned on the outside of the patients lips. Some variations of the hollow tube may further include an inner septum that divides the tube into first and second lumens that are connected at the distal end of the tube. Some variations of the hollow tube may provide an inner channel that that extends along the inner surface of the tube. The inner channel may be suitable for receiving a suction catheter, a catheter that can be used as a carbon dioxide or other gas sampling line, or a gastric tube. The suction catheter may be associated with a reservoir in which fluid removed from the hollow tube can be deposited. Some variation may provide a gastric tube that is attached and runs parallel to the pharyngeal tube.

A nasal cannula assembly is disclosed having a face mount part, in use resting against a user's face, which includes at least one nasal prong capable of being fitted into a person's nares. The cannula assembly also includes a manifold part, in fluid communication with the face mount part, having a single horizontal side gases entry. In particular, this cannula assembly is for supplying heated, humidified gases to a patient suffering from COPD. A tie or lanyard is disclosed for use with a breathing assistance apparatus such as a nasal cannula, face or nasal mask or tracheostomy connector. The tie or lanyard transfers the weight of the conduits supplying gases to the breathing assistance apparatus from the breathing assistance apparatus and distributes it onto the neck of the patient.

A process, a signal processing unit and to a ventilator automatically calculate a set point for a frequency, with which the ventilator performs ventilation strokes and thereby mechanically ventilates the patient. An alveolar or proximal minute volume is predefined. A lung time constant for the lungs of the patient is determined. The volume of a dead space in a fluid connection between the lungs and the ventilator is determined. A mandatory frequency set point (f.sub.set,mand) for the mandatory ventilation of the patient is calculated. An ideal frequency (f.sub.spon), with which the patient can achieve the minute volume by means of spontaneous breathing, is calculated. The ventilation frequency set point is calculated as a weighted average of the mandatory frequency set point (f.sub.set,mand) and of the ideal frequency (f.sub.spon). The averaging depends on a determined actual intensity of the spontaneous breathing of the patient.

A nasal cannula assembly is disclosed having a face mount part, in use resting against a user's face, which includes at least one nasal prong capable of being fitted into a person's nares. The cannula assembly also includes a manifold part, in fluid communication with the face mount part, having a single horizontal side gases entry. In particular, this cannula assembly is for supplying heated, humidified gases to a patient suffering from COPD. A tie or lanyard is disclosed for use with a breathing assistance apparatus such as a nasal cannula, face or nasal mask or tracheostomy connector. The tie or lanyard transfers the weight of the conduits supplying gases to the breathing assistance apparatus from the breathing assistance apparatus and distributes it onto the neck of the patient.