Abstract: A nebulizer system is disclosed, and comprises a first portion and a second portion configured for selectably receiving and electrically connecting to the first portion. The first portion includes a first housing for containing fluid, a vibratable mesh which seals a first outer opening of the first housing and configured to release fluid from the first housing through the first outer opening, first electrical conductors electrically connected to the vibratable mesh, a wick arranged such that vibration of the vibratable mesh causes release of fluid from the wick, and a biasing member compressing the wick against the vibratable mesh. The second portion includes a second housing having a second outer opening, second electrical conductors for contact with the first electrical conductors, and control electronics electrically connected to the second electrical conductors and configured to control the vibratable mesh to cause fluid release from the first housing through the outer openings.

Abstract: A portable electronic vaporizer for vaporizing product to be inhaled by a user of the vaporizer. The portable electronic vaporizer includes a mouthpiece, a product chamber, a heating element, a power source, and a mouthpiece.

Abstract: A full hood respirator includes a fluidtight flexible bag intended to be slipped over the head of a user, the flexible bag being equipped with a transparent window and comprising, in its lower part, a source of oxygen-enriched gas and connected to an outlet orifice opening into the internal volume of the flexible bag, characterized in that the hood comprises a flexible suspension member arranged inside the flexible bag, the suspension member forming a hat or cap having a surface area smaller than the surface area of the outer flexible bag, at least part of the border of the suspension member is rigidly connected to the flexible bag, the suspension member being intended, when the hood is in the position of use, to rest on the top of the head of the user at a height somewhere between the base and the top of the hood.

Abstract: This atomization unit is provided with a reservoir that holds an aerosol source, an atomization part that atomizes the aerosol source, and a cap body that blocks a supply port for supplying the aerosol source to the reservoir, wherein movement of the cap body away from the reservoir causes the atomization part and/or a power supply member, which electrically connects a power source and the atomization part, to break.

Abstract: A cushion tension assembly for a respiratory interface device is provided. Cushion tension assembly includes an adjustment assembly and a number of tension members. Each tension member is operatively coupled to the adjustment assembly and is operatively coupled to the cushion body. In this configuration, the adjustment assembly is structured to move cushion body between a first configuration in which the cushion body provides a generally continuous seal, and a second configuration in which the cushion body provides a more complete seal.

Abstract: Aspects of the subject technology relate to a control device for a medical ventilator. The control device has a user definable medical ventilator protocol and is configured to select a plurality of objects from a group of objects, wherein each of the objects are segments of the ventilator protocol, and each of the objects has at least one attribute. Further, the control device is configured to arrange the plurality of objects in a sequence, initiate the at least one attribute to define a property for each object in the plurality of objects, and execute the sequence. The medical control device gives the user flexibility to define and implement a medical ventilator protocol in a faster way than possible today and for different patients and/or ventilator situations.

Abstract: Systems and methods for detecting extubation of an endotracheal tube (ETT) are described. Extubation of the ETT can be identified by comparing to a threshold, a difference between a determined first volume of breathing gas during a first inspiratory period to a determined second volume of breathing gas during a second inspiratory period. If the difference exceeds the threshold, an alarm can be activated indicating extubation. Extubation detection may also be based on a difference between inspiratory pressures during separate inspiratory periods. Partial extubation and full extubation may also be discerned. Further, extubation of an ETT may be detected without the use of an exhalation flow sensor.

Abstract: To provide excellent skin touch feeling, a compression resistant and durable concavo-convex shape providing an uneven feeling, and excellent absorption performance, a sanitary napkin is provided that includes an absorber interposed between a permeable front surface sheet embossed into a concavo-convex shape and a back surface sheet and a hydrophilic third sheet disposed between the permeable front surface sheet and the absorber. The permeable front surface sheet is a laminate structure that includes a fine fiber skin contact surface layer made of fine fibers having a fineness of less than 2.0 dtex and a crimped fiber layer laminated on the non-skin contact surface of the fine fiber layer and the crimped fibers have a fineness of from 3.0 to 5.0 dtex.

Abstract: A respiratory mask can be used to provide therapy to patients who also require a nasogastric (NG) tube. The mask seal can include a path that is designed to deform around an NG tube or other without lifting the mask away from a patient's face. The deforming path can help to minimize gaps that form between the patient's face and the mask seal as a result of the tube, thus reducing leaks and improving the efficacy of the treatment.

Abstract: An aerosol-generating system(includes a cartridge, a liquid aerosol-forming substrate, and an aerosol-generating device. The cartridge includes a cartridge housing and a solid aerosol-forming substrate. The aerosol-generating device includes a cavity configured to receive at least a portion of the cartridge, an airflow inlet, and an airflow sensor. The airflow sensor is in fluid communication with the airflow inlet and the cavity). The aerosol-generating device includes a bypass air inlet in fluid communication with the cavity, an electric heater configured to heat the liquid aerosol-forming substrate, a power supply, and a controller. The aerosol-generating system is configured so that the cartridge housing substantially prevents airflow through the bypass air inlet when the cartridge is received within the cavity.

Abstract: A survival helmet device for use in combination with a survival suit includes a helmet, inhale and exhale control valves, and at least one inflatable air cavity pocket secured to the survival suit for selectively controlling the air supply and buoyancy of the survival helmet device and the survival suit.

Abstract: A bi-functional intubating and ventilating supraglottic airway includes a supraglottic bowl defining a distal end, a neck extending outward of the supraglottic bowl and defining a proximal end, and a longitudinally extending intubation conduit formed therethrough. The supraglottic bowl includes a cuff and defines a bowl surface, wherein the intubation conduit extends from the proximal end of the neck to an opening in the bowl surface, and wherein the intubation conduit is configured to have an endotracheal tube inserted therethrough. At least one fluid flow channel is formed longitudinally through a wall of the supraglottic airway, collaterally to the intubation conduit, from the proximal end to the bowl surface within the supraglottic bowl.

Abstract: A disposable absorbent article may include a chassis that includes a topsheet, a backsheet, and an absorbent core disposed between the topsheet and the backsheet; and a leg gasketing system. The leg gasketing system may include an inner cuff and an outer cuff; the inner cuff may include an inner cuff folded edge and an inner cuff material edge and the outer cuff may include an outer cuff folded edge and an outer cuff material edge such that the web of material is folded laterally inward to form the outer cuff folded edge and folded laterally outward to form the inner cuff folded edge. The leg gasketing system may also include a leg gasketing system pocket with an opening on an inboard longitudinal edge of the pocket.

Abstract: The present invention relates to oxygen sensors for medical ventilators. A medical ventilator includes a patient circuit delivering inspiratory airflow to a patient and returning expiratory airflow from the patient back to the ventilator. A manifold includes an air flow path into the patient circuit, and a port with an opening for an oxygen sensor. When mated to the port, the oxygen sensor samples the air in the air flow path and detects the amount of oxygen in the air. When the oxygen sensor is inserted into the port, a valve is biased open, to allow airflow through the opening into the oxygen sensor during ventilation. When the oxygen sensor is removed from the port, the valve biases into a closed position covering the opening, to prevent leaks. The ventilator can then continue to operate without the oxygen sensor in place.

Abstract: The present disclosure pertains to a system for controlling a leak flow rate during respiratory therapy. The system is configured to determine a leak flow rate necessary for CO2 expulsion for an individual subject and facilitate control of the leak flow rate during therapy such that the system exhausts substantially the entire exhaled volume of gas during an expiration of the subject. The system facilitates control of the leak flow rate during therapy via an adjustable leak valve. Determining the leak flow rate for the subject and facilitating control of the leak rate may minimize noise from air flow in the system, minimize the power draw needed by a pressure generator of the system, reduce a loss of medicine added to the respiratory therapy gas, and/or have other advantages, while still expelling the desired amount of CO2.

Abstract: A ventilator system and method can deliver artificial respirations to a person receiving cardiopulmonary resuscitation. The system and method may provide intermittent breath delivery (e.g., with interruptions), so that activation of the device gives a specific predetermined number of breaths, interspersed with a set time period of no breath. This pattern may be by default, manually triggered where one activation gives a set number of breaths followed by a pause until the next activation for breath (one activation gives one breath cycle), or one activation results in continuous cycle of intermittent breaths). In some embodiments, a signaling mechanism may deliver signals to a rescuer relating to timing of chest compressions of the person. The timing of the chest compressions for the signals may be based on a time of delivery of the artificial respirations. In certain embodiments, different sized masks each include a gas flow restrictor which is unique for the size of mask.

Abstract: Apparatuses, components, methods, and techniques for altering equipment operation are provided. An example tool control and breathable air delivery system includes equipment including a tool and a controller configured to control the tool. The example system also includes a wearable respirator and an air delivery device connected to the wearable respirator. The example system further includes an air evaluation monitor configured to generate a signal based upon a condition of air being delivered to the wearable respirator. An example electronic circuit is configured to adjust the tool based at least in part on the signal generated by the air evaluation monitor. An example method includes enabling the tool, providing air to a respirator, determining a condition of the air, and adjusting the tool based on the condition of the air.

Abstract: A respiratory assisting device comprising of an expandable bag which has a bilayer that can be inflated in order to give the bag a rigid and predetermined shape. The bag can then be compressed in order to displace inspiratory gas that is in the inner cavity and deliver it to the patient. The bag includes a one-way valve that passes through the bilayer allowing the inner cavity of the bag to fill with ambient air when the air within the cavity has been expended. The bag portion is connected to an air-tight hollow wall prism shape enclosure via a T-connector piece. This t-shaped connecting piece allows the air to pass through two manifold chambers that attach to another t-shaped connecting piece.

Abstract: A respiratory therapy apparatus includes components operable to simultaneously provide a High Frequency Chest Wall Oscillation (HFCWO) therapy and a Mechanical Insufflation/Exsufflation (MIE) therapy to a patient. The respiratory therapy apparatus includes a controller that controls a synchronization of the HFCWO therapy and the MIE therapy to provide respiratory therapy to the patient to effectively clear mucous or induce deep sputum from the lungs of patient.

Abstract: An elbow connector (10,20) for use with a patient interface device (2) includes a coupling portion (11,21) structured to be inserted into an opening in the patient interface device to couple the elbow connector with the patient interface device. The coupling portion includes an upper coupling portion (11a) and a lower coupling portion (11b). The elbow connector also includes a rear surface (13). Applying pressure to the rear surface causes the upper coupling portion to move towards the lower coupling portion.