Training device for training tracheal suctioning. The training device includes a tracheal core adapted to be arranged within a tracheal, nasal or oral cavity of a medical training simulator, and coupled to the airways of the simulator and an insert adapted to be inserted into the core, the insert forming a reservoir for simulated mucus.

An automated system, method or computer program product for providing visual recognition and counting of drops falling into a drip chamber for intravenous therapies (drip rate). The Automatic Visual Recognition Intravenous Infusion Drop Counting Application software subroutine framework can run on a mobile device and can be configured to, when activated, calculate and visually recognize the drip rate of intravenous therapies. The functionality of the Automatic Visual Recognition Intravenous Infusion Drop Counting Application software subroutine framework allows the user to manage standard drip sets. Additionally, different drip set values can be assigned. The Automatic Visual Recognition Intravenous Infusion Drop Counting Application software subroutine framework also allows the user to manage the infusion; application can integrate a timer and other diverse features. The updated information can be stored in the internal memory of the device, other information recording medium, a memory data storage device or into a web based storage service.

Disclosed is an ambulatory infusion device, including a control unit and an electroacoustic transducer. The control unit is configured to operate the electroacoustic transducer as noise emitter or to operate the electroacoustic transducer as noise receiver and to determine from a received noise that is received by the electroacoustic transducer a state of the ambulatory infusion device.

A vaporization device allow users to consume removable cartridges filled with vaporizable material. The vaporizer devices defines a receptacle shaped to receive a cartridge in a snug and compact nesting arrangement. The vaporizer device ensures that the installed cartridges are secured and provide a sealed fluid path. The cartridges have wider fluid conduits facilitating user inhalation. The cartridges also facilitate manufacturing by providing a larger area within which to insert the vaporizable material.

[Subject] A test substance application system for animal experiment capable of administering a required amount of a test substance uniformly and reliably from a nose or a mouth into a nasal cavity or into a lung of an experimental animal is provided. [Means for Solution] The system includes a respiration monitoring device 2 that monitors a respiration state of an experimental animal detected by a respiration pick-up device 1 to thereby measure a timing upon switching from an expiratory phase to an inhalatory phase and outputs a trigger signal T at that timing, and an application device 3 that sprays a predetermined amount of a test substance into a nasal cavity or an oral cavity of the experimental animal when the trigger signal T is outputted from the device 2.

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 flow restriction element (35) for controlling the passage of gas from the second compartment (2) to the first compartment (1).

In an embodiment, a metered dose inhaler (MDI) training device is provided herein. The MDI training device may include a housing having an inhalation port, an opening for receiving ambient air, the inhalation port and the opening are fluidly connected to provide an air flow channel, and a valve associated with the air flow channel, the valve having an opened state and a closed state, and an actuation member, wherein the valve is not allowed to enter the opened state if the actuation member is actuated prior to inhalation through the inhalation port.

An interfacing structure is arranged to cooperate with a frame to contact with the skin of a patient. The interfacing structure includes a clip portion joined to a cushioning component. The frame is more rigid than the clip portion and the clip portion is more rigid than the cushioning component.

An apparatus for extracorporeal treatment of blood (1) comprising a treatment unit, a blood withdrawal line, a blood return line, a preparation line and a spent dialysate line. A control unit (10) is configured to calculate values of a parameter relating to treatment effectiveness based on measures of the conductivity in the spent dialysate line. The value of the effectiveness parameter is calculated using one or more values representative of the conductivity in the spent dialysate line obtained relying on a mathematical model.

A medication concentration detecting device includes a medicine container, a three-way pipe, a light emitting member, a first light receiver and a processor. The medicine container has a chamber configured for accommodating nebulized medicine. The three-way pipe has a passageway connected to the chamber for the nebulized medicine to flow along the passageway. The light emitting member is disposed on the three-way pipe and configured for emitting a light beam toward the passageway. The first light receiver is disposed on the three-way pipe and configured for receiving the light beam and outputting a luminous flux signal. The processor is connected to the first light receiver and configured for calculating a luminous flux reference value according to the luminous flux signal. The luminous flux reference value is used for determining whether outputs a low nebulized medicine concentration warning.