The present invention relates to the technical field of an automatic detection trigger device, and discloses an automatic detection trigger device for a quantitative compressed administration aerosol. The automatic detection trigger device for the quantitative compressed administration aerosol includes a main machine body, wherein the main machine body consists of a main machine front cover, a main machine rear cover, a battery module and a driving assembly; the driving assembly includes a driving control module and a driving gear module; a charging port is formed at an outer side of the main machine front cover; a limiting pedestal is clamped at a bottom end of the main machine front cover; and an aerosol medicine is fixedly mounted at the bottom of an inner cavity of the main machine front cover. The automatic detection trigger device for the quantitative compressed administration aerosol detects an inspiration flow rate of a user in a medicine inhaling process through a flow sensor arranged in the driving assembly. When the inspiration flow rate reaches an ideal threshold, the device drives the aerosol to spray a medicine, and the medicine sprayed by the aerosol enters a lower respiratory tract such as a lung along with airflow, so that the problem of hand-mouth synchronous operation is solved, and the utilization rate of the medicine is greatly increased.

An apparatus for delivery of a flow of gases to a user, such as a respiratory therapy apparatus, is provided. The apparatus may have first and second inlets for receiving supplementary gases flows, a blower to generate the gases flow to the user, and a controller. A valve and a sensor may be provided in the second inlet. The controller may be configured to detect the disconnection of a gases source from the second inlet, and to respond by operating the valve and/or triggering an alarm. The controller may be configured to determine whether a gases flow is being provided at one or both of the inlets, and to accordingly control an operational mode of the apparatus.

A fluid handling cassette, such as that useable with an automated peritoneal dialysis (APD) cycler device or other infusion apparatus, may include a generally planar body having at least one pump chamber formed as a depression in a first side of the body and a plurality of flowpaths for a fluid that includes a channel. A patient line port may be arranged for connection to a patient line and be in fluid communication with the at least one pump chamber via at least a first one of said flowpaths, and an optional membrane may be attached to the first side of the body over the at least one pump chamber. In one embodiment, the membrane may have a pump chamber portion with an unstressed shape that generally conforms to the depression of the at least one pump chamber in the body and is arranged to be movable for movement of the fluid in a useable space of the at least one pump chamber. One or more spacers may be provided in the at least one pump chamber to prevent the membrane from contacting an inner wall of the at least one pump chamber. The patient line, a drain line, and/or a heater bag line may be positioned to be separately occludable in relation to one or more solution lines that are connectable to the cassette.

A system for injection includes a syringe body having proximal and distal ends, a syringe interior, and a syringe flange at the proximal end thereof. The system also includes a stopper member disposed in the syringe interior. The system further includes a plunger member coupled to the stopper member and configured to be manipulated to insert the stopper member distally in the syringe interior relative to the syringe body. Moreover, the system includes a needle coupled to the syringe body at the distal end thereof. In addition, the system includes a smart flange removably coupled to the syringe body. The smart flange includes a mounting sensor to measure mounting data. The smart flange also includes a processor to analyze the mounting data to determine the presence and the type of the syringe body disposed in the smart flange.

Provided is an aerosol generating system including a holder configured to generate aerosol by heating a cigarette; and a cradle including an inner space into which the holder is inserted. The holder is configured to be tiltable with respect the cradle. The holder is inserted into the inner space of the cradle and then tilted to generate the aerosol.

In one aspect, a medical device includes: a housing; a plurality of attachment points disposed on a face of the housing and configured to hold a medical fluid tubing system; a lighting system disposed at or below the face of the housing; and a processor configured to control the lighting system to (a) visually indicate the locations of the attachment points and (b) in response to a feedback signal indicating whether or not the medical fluid tubing system is attached to at least one of the attachment points, alter the visual indication of the lighting system.

An electronic module for an inhaler includes a printed circuit board and electronic components configured to detect at least a status and/or at least a working parameter of the inhaler when the electronic module is attached to the inhaler. A battery is permanently joined to the printed circuit board. A first terminal and a second terminal are electrically connectable one to the other through a main switch to close a circuit between the battery and the electronic components. In a rest configuration, the first and second terminals are electrically separated by the main switch. In a work configuration, the first terminal and the second terminal are electrically connected one to the other through the main switch.

An apparatus for treatment of a respiratory condition, the apparatus comprising: a pressure generator configured to generate a flow of breathable gas; an intermediate component pneumatically connected to an air delivery tube, the intermediate component comprising a port configured to facilitate propagation of sound outside of the intermediate component; a sensor attached externally to the intermediate component and located adjacent to the port of the intermediate component, the sensor configured to sense sound propagated through the air delivery tube; and a controller. The controller can be configured to: receive a sound signal generated by the sensor as a result of sensing sound during operation of the apparatus, analyse the received sound signal, and effect a response based at least in part on the analysing.

The invention relates to a blood treatment device, having the following:

a fluid line system (10) for guiding a fluid flow comprising a line portion (14), wherein the line portion (14) can be formed as a closed fluid system, and comprising at least one first concentrate supply line (26) for supplying a first concentrate solution; a fluid pump (11) for conveying the fluid in the fluid line system (10); a determining means (13; 23; 33; 29) for capturing a state of the fluid line system (10); a control unit for controlling the fluid flow; characterized in that the control unit is configured in such a way that the line portion (14) only forms a closed fluid system when the state captured by the determining means (13; 23; 33; 29) meets a predetermined condition.

Apparatus for recording information concerning the use of an injection device, the apparatus comprising: one or more sensors for providing information indicative of how the injection device is used; a processor configured to analyse said information detected by the one or more sensors to determine use information, said use information corresponding to how the injection device is used; and a memory for storing said use information in an image format such that said use information can be retrieved from the memory and displayed in an image.