A medical fluid pump of the infusion or syringe pump design includes a fluid pump housing which includes a display unit, in particular a display or touch display, with a plurality of display panels that are prepared and configured to display at least one respective function parameter of the fluid pump, including at least one setting parameter which can be set directly by a user of the fluid pump and a plurality of operating parameters which cannot be set directly by the user. The representation of the at least one setting parameter stands out visually against the operating parameters, such as by displaying the at least one setting parameter in an enlarged size compared to the operating parameters.

A medical pump for conveying a medical liquid has a pump housing and a front lid hingedly arranged at the pump housing. The medical pump also has a lid housing and an operating element integrated in the lid housing. The operating element features a resistive touch element and a separate display element arranged at a parallel distance to the touch element. The touch element and the display element jointly form a touch screen, and are fastened at respectively opposing sides of the lid housing.

A medical pump system includes at least one medical fluid pump of a first type and at least one medical fluid pump of a second type. The medical fluid pumps can be assembled or arranged vertically, with one of the medical fluid pumps positioned above the other. Each medical fluid pump has a movable front flap with an integrated display and operating elements. The medical fluid pumps can be directly connected to one another in a vertical arrangement, or arranged in a vertical arrangement with the aid of a carrying or holding device. When the medical fluid pumps are vertically arranged, the displays and operating elements of the respective medical fluid pumps are aligned vertically.

Devices, systems, and methods for monitoring respiration using surface temperature, humidity, air pressure, carbon dioxide gas sensors, pulse oximetry sensors and electromyography sensors, and/or acceleration sensors to obtain information related to respiration rate (RR), exhalation/inhalation strength, exhalation/inhalation volume, exhalation/inhalation acceleration, and/or exhalation/inhalation regularity.

An aerosol generating device includes a heater that heats an aerosol generating substrate, a temperature sensor that detects a temperature of the heater, and a controller that controls power supplied to the heater through a power signal such that the heater is heated within a preset temperature range, filters the power signal, and detects a user's puff based on the filtered power signal. Accordingly, the aerosol generating device according to the present disclosure may more accurately detect a user's puff.

The operational parameters of a respiratory apparatus can be controlled through the use of a user interface located on a separate or separable mobile computing device. Sensors or features located on the mobile computing apparatus can be used to adjust the operation parameters or therapy of the respiratory apparatus or otherwise improve the compliance of a patient utilizing the respiratory apparatus.

A wearable health and lifestyle device including at least a measurement module configured to be worn by a user in at least a first wearing position, the measurement module comprising a 3-axis accelerometer unit configured to provide acceleration data and inclination data, a temperature measurement unit configured to provide temperature data, a light radiation measurement unit configured to provide light radiation data, said light radiation measurement unit comprising at least one multi-spectral sensor configured to measure wavelength bands over the range 290 nm to 1150 nm, a storage module configured to receive and store said acceleration data, said inclination data, said temperature data and said light radiation data, and an analysis module configured to analyze a data set comprising acceleration data, inclination data, temperature data and light radiation data.

Embodiments of the disclosure provide a transfusion guiding robot and a guiding method for guiding a movement of a transfused person. The transfusion guiding robot comprises a controller, a moving portion and a fixing portion. The controller is configured to receive and process instruction information, and control the transfusion guiding robot according to the instruction information; the moving portion is configured to move according to a command from the controller; and the fixing portion is configured to fix a container, a height of the fixing portion being adjustable.

An overdose of opioids can cause the user to stop breathing, resulting in death. A physiological monitoring system monitors respiration based on oxygen saturation readings from a fingertip pulse oximeter in communication with a smart mobile device and sends opioid monitoring information from the smart mobile device to an opioid overdose monitoring service. The opioid overdose monitoring service notifies a first set of contacts when the opioid monitoring information.

A resuscitation management system for a manual resuscitator may include a radio frequency identification (RFID) tag that may be configured to be mounted on a first side of a bag of the manual resuscitator. The RFID tag may be configured to transmit information indicative of the presence of the RFID tag. The system may further include an RFID reader that may be configured to be mounted on an opposite second side of the bag. The RFID reader may be configured to generate an output signal corresponding to the presence of the RFID tag responsive to receiving the information transmitted by the RFID tag. The RFID reader may be configured to receive the information transmitted by the RFID tag responsive to the RFID tag being at a distance from the RFID reader smaller than a predetermined threshold.