Abstract: A protective shield is provided for covering a self-contained breathing apparatus (SCBA) mask or a full-face air purifying respirator (APR) lens to prevent damage and scratching. The shield consists of a die cut shape of thermoplastic sheet that duplicates the outline of the self-contained breathing apparatus mask lens and/or frame. The protective shield can be produced using various grades, colors and/or densities of material replicating limited visibility or blackout conditions. To protect the majority of the plastic lens, the shape of the shield includes a peripheral overlap onto the mask utilizing the SCBA lens frame. The shield can be attached to the self-contained breathing apparatus face mask by means of any of the following: bungee, hook, or elastic cord; all of which allows the shield to be attached or removed quickly. Many SCBA/APR training exercises require limited visibility.

Abstract: Apparatus for generating a supply of air at positive pressure for the amelioration or treatment of a respiratory disorder comprising a housing, a blower structured and configured to produce a flow of air at positive pressure, a flexible connector electrically and physically connected to the blower; and a blower rotation limitation structure configured to reduce rotation of the blower during use. The apparatus may comprise first and second blower suspensions for holding opposite ends of the blower. The blower suspension(s) may be flexible and in tension. The apparatus may comprise one or more connector anchors for anchoring a longitudinal middle section of the flexible connector to another part of the apparatus.

Abstract: Systems and methods are provided for delivering one or more drugs. In some embodiments, a drug delivery system includes a housing having a distal end with an inlet through which an inspiratory flow of air passes into the housing, a proximal end having a patient interface attached thereto, the patient interface being configured to interface with a user, and an inspiratory flow pathway extending from the distal end to the proximal end of the housing. A nitric oxide (NO) source is positioned within the housing and is configured to deliver NO-containing gas to the patient interface. A secondary drug source is positioned within the housing and is configured to deliver a secondary drug to the patient interface. A controller is configured to control an amount of NO-containing gas and an amount of the secondary drug delivered using a control scheme.

Abstract: An emergency ventilation system ventilates a patient and includes a chamber housing defining a breathing chamber; a piston; and a motor operably connected to the piston. The motor applies an exhalation force to move the piston in an exhalation direction applies an inhalation force to move the piston in an inhalation direction. The piston increases air in the breathing chamber as the exhalation force is applied and decreases air in the breathing chamber as the inhalation force is applied. An exhalation check valve allows airflow from the air source to the breathing chamber and not to allow airflow from the breathing chamber to the air source as the inhalation force is applied. An inhalation check valve allows airflow from the breathing chamber to the air output and not to allow airflow from the air output to the breathing chamber as the exhalation force is applied.

Abstract: The invention relates to a breathing assistance apparatus that may be configured to reduce the risk of damage to electronics within the apparatus as a result of liquid leaks within the apparatus or impacts to the apparatus. In other forms, the apparatus may be configured to allow for easy assembly and/or safe operation.

Abstract: There is described a ventilator for ventilating an airway of a patient. The ventilator is generally configured to perform a series of respiration cycles, wherein each respiration cycle includes the delivery of a main volume of fresh respiratory gas into the patient's airway, followed by the evacuation of a corresponding volume of used respiratory gas, and to further perform a series of subcycles during a corresponding one of the respiration cycles, wherein each subcycle includes the delivery of an auxiliary volume of fresh respiratory gas into the patient's airway, followed by the evacuation of a corresponding volume of used respiratory gas, the auxiliary volume being smaller than, and distinct from, the main volume.

Abstract: A foot stretching/checkup device includes: a motor unit; a footrest unit including a lower footrest configured to be rotated about a first rotation axis, an upper footrest configured to be rotated about a second rotation axis and a connecting member connecting the upper footrest and the lower footrest; and a coupling unit including an arm portion rotated by the motor unit and a rotary coupler coupled to the upper footrest. The upper footrest is configured to be rotated by a predetermined angle about the second rotation axis by the rotation of the arm portion. The lower footrest is configured not to be rotated about the first rotation axis by rotation of the arm portion until the upper footrest is rotated by the predetermined angle.

Abstract: A hair and scalp treatment device includes a dispenser connected to a cartridge, wherein the cartridge comprises a formulation; a plurality of tips on the device, wherein the tips have at least one opening to dispense the formulation and at least one LED that emits light in the visible color spectrum, wherein the at least one LED is located at the end of the tips; and a controller configured to individually turn on and off the LEDs from the plurality of tips.

Abstract: A resuscitation chamber apparatus for administering hyperbaric oxygen to a patient. More particularly, the present invention relates to a hyperbaric oxygen compatible critical care chamber apparatus preferably for use in emergency departments and/or prehospital ambulance management of patients. In a preferred embodiment of the present invention, the apparatus is a resuscitation monoplace hyperbaric chamber preferably used in critical care management of acutely ill or injured patients in prehospital emergency medical services (EMS) settings or in hospital emergency departments. The apparatus preferably allows a critical care shock or arrested patient to be pressurized preferably without compromise for application of best medical equipment, medications and human resuscitating intervention.

Abstract: A nitric oxide administration device 1 includes a first flow path 101 including a first intake port 101a and an oxygen supply port 101b, an oxygen generation unit 100 which is arranged in the first flow path 101 and which generates concentrated oxygen from air introduced via the first intake port 101a, the generated concentrated oxygen being supplied via the oxygen supply port 101b, a second flow path 201 which is branched from the first flow path 101 and which includes an NO supply port 201b, and an NO generation unit 200 which is arranged in the second flow path 201 and which generates NO from gas distributed from the first flow path 101, the generated NO being supplied via the NO supply port 201b.

Abstract: The present disclosure relates to a breathing assistance apparatus for providing a breathing assistance to a user. The breathing assistance apparatus includes a first/second source configured with a first/second buffer. The first/second fluid is controllably transferred from the first/second source to the first/second buffer using any or combination of a first/second pressure regulators and one or more first/second valves. A mixing chamber configured with the first buffer and the second buffer to receive and mix the first fluid and the second fluid. A delivery tank configured with the mixing tank to controllably receive the third fluid through one or more fourth valves and a third pressure regulator. A user feed mask having an inlet configured with the delivery tank and user's face facilitating breathing assistance to the user.

Abstract: A cushion member for use in a patient interface device for delivering a flow of breathing gas to an airway of a patient includes a plurality of dimples defined in a portion of the cushion member.

Abstract: Methods and systems are provided for an oxygen sensor included in a medical gas flow device, such as an anesthesia machine. In one embodiment, a method for a medical gas flow device comprises tracking an output voltage of an oxygen sensor during calibration over time, and, responsive to the output voltage decreasing by at least threshold amount from an initial calibration output voltage, estimating an end-of-life date of the oxygen sensor and outputting a replacement notification.

Abstract: A mobile oxygen point of use apparatus includes a standalone and portable mounting panel having a first side and a second side and is configured to be portably relocated within a facility by at least one human operator. A first set of oxygen flow regulators are mounted on the first side of the mounting panel and have multiple first oxygen inputs and multiple first oxygen outputs. A second set of oxygen flow regulators are mounted on the second side of the mounting panel and have multiple second oxygen inputs and multiple second oxygen outputs. A low pressure oxygen input is mounted on the mounting panel and a single pipeline or hose is configured to be connected from the low pressure oxygen input to a source of oxygen. Distribution plumbing connects the low pressure oxygen input to the multiple first oxygen inputs and the multiple second oxygen inputs.

Abstract: A pressure controller 1 supplies fluid to a cuff and controls an internal pressure of the cuff. The pressure controller 1 has a housing 10 having a flattened shape. In the housing 10, a pump 31 having a discharge port 33 through which the fluid is discharged and which is directed in a thickness direction of the housing 10, and a control module 20 which controls the pump 31 such that the internal pressure of the cuff falls within a predetermined range, are disposed. A filter 39 which has elasticity and has lower thermal conductivity than the housing 10 is disposed at a side opposite to the discharge port 33 and between the pump 31 and an inner surface of the housing 10.

Abstract: A patient interface comprises an opening for receiving a flow of gas from a conduit and an adaptable connector system for connecting at least two different types of conduit with the opening. The adaptable connector is permanently mounted with the patient interface so it cannot be lost and is able to swing into alignment with the opening, thereby providing a different connection end to be compatible with a second or further type of conduit connection end.

Abstract: An active humidifier includes a disposable cartridge provided with a humidification chamber adapted to contain water to be heated for air humidification, with an inlet mouth for air introduced by a ventilation device and with an outlet mouth for conditioned air to a patient, the cartridge includes a disposable heating element directly inserted inside the humidification chamber close to the bottom and distanced therefrom, immersed in the water and lapped on all sides, the cartridge also includes an electrical connector for the electrical connection of the disposable heating element, and the disposable heating element includes an electrical resistor and in the humidification chamber is a sealed casing entirely made of plastic material.

Abstract: An anesthesia machine, an anesthetic output concentration monitoring method, system, a device, and a storage medium are disclosed. The method includes respectively monitoring a flow of a fresh gas flowing into a breathing circuit and a flow of an inhaled gas of an anesthetized object. The method further includes when the inhaled gas flow is greater than a fresh gas flow, respectively monitoring a concentration of anesthetic in the inhaled gas and an exhaled gas of the anesthetized object. The method also includes using the exhaled gas anesthetic concentration and a concentration of carbon dioxide in the exhaled gas to calculate a concentration of anesthetic in a gas, reflowing into an inspiratory branch, in the exhaled gas, thereby obtaining a re-inhaled gas anesthetic concentration.

Abstract: Medical tubes and methods of manufacturing medical tubes are disclosed, such as in positive airway pressure (PAP), respirator, anaesthesia, ventilator, and insufflation systems. The tube may be a composite structure made of two or more distinct components spirally wound to form an elongate tube. One of the components may be a spirally wound elongate hollow body, and the other component an elongate structural component spirally wound between turns of the spirally wound hollow body. Alternatively, the tube need not be made from distinct components. For instance, an elongate hollow body formed (e.g., extruded) from a single material may be spirally wound to form an elongate tube. The elongate hollow body itself may in transverse cross-section have a thin wall portion and a relatively thicker or more rigid reinforcement portion. The tubes can be incorporated into a variety of medical circuits or have other medical uses.

Abstract: A panel for covering a supply channel in a passenger cabin of a vehicle including a mounting surface facing the passenger cabin while the panel covers the supply channel. The panel is elongated in a longitudinal direction and adapted for mounting passenger supply units. The mounting surface includes spaced openings arranged along a longitudinal direction of the panel, wherein each opening includes a connector assembly for a passenger supply unit. The panel includes a mount securing passenger supply units. The mounting surface comprises extended areas for providing support in opposing lateral directions to passenger supply units mounted to the panel.