An apparatus (1) for supplying a gas mixture to a patient, having a gas inlet line (30) with a gas inlet orifice (30a) that splits into a first gas line (31) and a second gas line (32); at least one permeation module (33) arranged on the second gas line (32), the said permeation module (33) having a feed port (33a) in fluidic communication with the second gas line (32), a retentate port (33b) and a permeate port (33c); a third gas line (34) in fluidic communication with the retentate port (33b) of the permeation module (33); a fourth gas line (35) in fluidic communication with the permeate port (33c) of the permeation module (33), and coupling fluidically to the said first gas line (31); and a source (360) of air in fluidic communication with the first gas line (31) and the fourth gas line (35).

A method for manufacturing a filter (1) for gas masks includes providing a flat paper and folding the paper into a pleated preform. The filter element (2) is separated from the pleated preform (6) and is inserted into a housing (3). The inserted filter element (2) is connected to the housing (3) at least at some points. This filter elements (2) may have a polygonal outer contour, upon separating the element from the pleated filter preform (6). A foam and/or an adhesive is applied to an outer edge of the filter element (2), arranged on the circumference of the filter element, for an at least partial sealing of an edge (5). This establishes a connection to the housing (3) in at least some sections.

A breathing assistance apparatus is configured with features that improve serviceability of the apparatus. The apparatus can include animations to provide instruction regarding correcting easily-identified fault conditions and to provide instruction regarding routine maintenance routines. The apparatus also can be configured with top level control menus that are obscured in a manner to limit manipulation of the top level control elements by unauthorized users.

Apparatus and methods provide system characterisation such as for operation of respiratory treatment apparatus. Such a characterisation may include a determination of a patient interface type and/or an event such as a leak or blocked vent. For a characterisation, one or more controller(s) or processor(s) may be configured to make a determination of parameters that best fit a template curve, such as a quadratic function, to a plurality of measurements, such as data points. Each data point may include a pressure value, and a flow rate value at the pressure value. Parameters from the function may then be applied, such as with a data structure to characterize the system, such as with an identification of the patient interface type from the parameters. In some versions, parameter(s) of operation of the apparatus may be adjusted based on the characterisation, such as by using the parameters of the template.

An adapter (1) for establishes a flow channel (2) between a breathing gas supply and a patient connection piece. A set (20) and a system (30) for ventilation or respiratory support, each include the adapter (1). The adapter (1) includes a first connection structure (3) configured to connect to the breathing gas supply and a second connection structure (4) configured to connect to a patient connection piece. A bypass channel (5) branches off from the flow channel (2) and is provided with an extraction opening (7) which can be closed at least temporarily by a safety valve (6). The safety valve (6) is configured such that the extraction opening (7) is closed when a ventilation pressure prevailing in the flow channel (2) is lower than a pressure prevailing on a side of the safety valve facing away from the flow channel (2).

A system for providing continuous positive air pressure therapy is provided. The system includes a flow generator, a sensor, and a computing device. The computing device is configured to control operation of the flow generator based on sensor data. The computing device is further configured to display, on a display device, one or more questions relating to demographic and/or subjective feedback; responsive to displaying the one or more questions, receive one or more inputs indicating answers to the one or more questions; transmit the answers to a remote processing system; receive, from the remote processing system, settings determined based on the transmitted answers; and adjust control settings of the system based on the received settings.

A sedation device (1) has a housing (2) having a ventilator chamber (3) and an associated patient chamber (4) in communication with the ventilator chamber (3). A filter (5) is mounted between the ventilator chamber (3) and the patient chamber (4) and forms a common gas-permeable dividing wall between the ventilator chamber (3) and the patient chamber (4). An inlet port (6) is provided on the ventilator chamber (3) for connection via a Y-piece to a ventilator. An outlet port (9) of the patient chamber (4) connects via a patient breathing tube (10) with a patient. An associated pair of inserts are provided, namely a first insert (14) fixedly mounted in the ventilator chamber (3) and a second insert (15) fixedly mounted in the patient chamber (4). One or both of these inserts (14, 15) are mounted within the housing (2) to vary the internal volume of the housing (2) as required to suit different patients. The inserts (14, 15) are nestably engageable with an inner wall of the housing (2).

The present invention relates to the art of automatic regulation of pulmonary devices for imitating, assisting and/or enforcing the breathing process by converting Bag-Valve-Mask (BVM) or a similar device to enhance both phases of breathing: inhalation and exhalation while applying a variable pressure during the breathing process. It also replaces a mechanical chest compression to the sternum area for automatic pneumatic compression, and it could be complimented with the use of a Tens unit, can be used for extended period of time with a high level of reliability, simplicity, efficacy and low cost. The unique filtration system's goal in this invention is safety of the treating patient as well as assisting personnel. This portable and light device is recommended to be used as a resuscitator for the patients with mild to extremely suppressed or without respiratory drive. The source of power can be electrical, battery operated, manual or a combination thereof.

A nasal delivery device for delivering substance to a nasal cavity of a subject, the delivery device comprising: a substance supply unit for supplying a dose of substance to be delivered to the nasal cavity of the subject, the substance supply unit including an inlet and an outlet; a nosepiece unit including a nosepiece for fitting to a nasal cavity of the subject and being in fluid communication with the outlet of the substance supply unit; and a mouthpiece unit including a mouthpiece in fluid communication with the inlet of the substance supply unit and through which the subject in use exhales such as to entrain substance from the container chamber and deliver the same through the nosepiece, and at least one temperature modifier for reducing a temperature of the exhaled air flow such as to reduce the absolute humidity thereof.

A respiratory therapy system can have a flow generator adapted to provide gases to a patient. A gas passageway can be located in-line with the flow generator. The gas passageway can have a first portion adapted to receive a first gas and a second portion adapted to receive a second gas. The gas passageway can have a static mixer downstream of the first and second portions.