A system for priming an infusion pump is disclosed. The system includes a priming cap including a septum and configured to matably connect with a male part comprising a needle and attached to a length of tubing for fluid, wherein when matably connected with the male part, the priming cap occludes the tubing.

A plunger assembly is configured for slidable advancement through a reservoir of a vessel containing a material to be administered. The plunger assembly includes a plunger rod having a distal end configured to be inserted into the reservoir. An elastomeric plunger extending from the distal end of the plunger rod is configured to sealingly engage a sidewall of the reservoir. At least one printed circuit board is embedded within the plunger, and at least one electronic component is electrically connected with the at least one printed circuit board.

Provided is an aerosol generation device that suppresses the effect that errors in the production of structural elements have on the accuracy with which shortage of an aerosol source is detected. An aerosol generation device that comprises: a power source; a load that has a temperature-variable electrical resistance value and atomizes an aerosol source by generating heat due to supply of power from the power source; a first circuit that is used for the load to atomize the aerosol source; a second circuit that is connected in parallel to the first circuit, has a higher electrical resistance value than the first circuit, and is used to detect voltage that changes as a result of changes in the temperature of the load; an acquisition part that acquires the value of voltage that is applied to the second circuit and the load; and sensors that output the value of the voltage that changes as a result of changes in the temperature of the load.

At least one example embodiment discloses a pod for an electronic vapor (e-vapor) apparatus. The pod includes a pre-vapor formulation compartment configured to hold a pre-vapor formulation therein, a device compartment in fluidic communication with the pre-vapor formulation compartment, the device compartment including a processor configured to monitor the pre-vapor formulation compartment and identify the pre-vapor formulation and a vapor channel extending from the device compartment and through the pre-vapor formulation compartment.

Fluid couplings prevent or discourage misconnection of fluid lines. In embodiments, a coupling device includes multiple male and female connectors that are joined to a common line. The coupling device is mated to a matching coupling device only when all the multiple male and female connectors are properly joined. If any of the connectors is not properly mated to a corresponding one, the coupling will leak, since the connectors on each side are joined to a furcating channel. In embodiments, the coupling devices are made unique by providing an arrangement of the connectors, number of connectors, shape of connectors or arrangement of interfering connector parts that ensure that any attempt to improperly couple two fluid lines will result in the incomplete mating and thereby cause leakage of the fluid, failure of the coupling to engage, or otherwise cause the attempt to connect to fail.

A disposable filter (100), for use in a breathing circuit of a ventilator, includes a filter housing (110), which encloses a filter material (112) of the disposable filter. The filter housing has a first filter opening (118) and a second filter opening (119) for the respective connection of a gas-carrying (gas-guiding) component, especially of a respective tube, for a gas to be carried through the disposable filter. The filter material is arranged between the first filter opening and the second filter opening. The disposable filter has on the filter housing an imprint (120), which is arranged on the filter housing by a printing process, and which forms a structured surface (122). The structured surface can be written on and includes at least seven check (marking) areas (124).

A method of detecting a hand-to-mouth (HMG) gesture with an e-vaping device includes detecting movements of the e-vaping device; generating quaternions based on the detected movements; generating movement features based on the generated quaternions; applying the generated movement features to a classifier; and determining whether the detected movements correspond to an HMG based on an output of the classifier.

Therapy gas delivery systems that provide run-time-to-empty information to a user of the system and methods for administering therapeutic gas to a patient. The therapeutic gas delivery system may include a gas pressure sensor attachable to a therapeutic gas source that communicates therapeutic gas pressure data to a therapeutic gas delivery system controller, a gas temperature sensor positioned to measure gas temperature in the therapeutic gas source that communicates therapeutic gas temperature data to the therapeutic gas delivery system controller, at least one flow controller that communicates therapeutic gas flow rate data to the therapeutic gas delivery system controller, at least one flow sensor that communicates flow rate data to the therapeutic gas delivery system controller, and at least one display that communicates run-time-to-empty to a user of the therapeutic gas delivery system. The therapeutic gas delivery system controller of the system includes a processor that executes an algorithm to calculate the run-time-to-empty from the data received from the gas pressure sensor, temperature sensor, flow controller and flow sensor, and directs the result to the display.

An assembly for a drug delivery device, the assembly comprising: a housing unit, the housing unit comprising a housing for receiving a reservoir and a dispensing mechanism configured to dispense liquid drug content from the reservoir in a dispensing operation, a cap which is releasably connected to the housing unit, the cap, when connected to the housing unit, at least partially covers a distal dispensing end of the assembly, which is uncovered when the cap is disconnected from the housing unit, a first information feature having coded first content, wherein the first information feature is machine-readable to retrieve the first content from the first information feature, a second information feature, wherein the first information feature is visible and/or machine-readable when the cap is connected to the housing unit and removable together with the cap from the housing unit or rendered unreadable when the cap is disconnected from the housing unit.

A processor associated with a respiratory therapy device (7040) applies acoustic techniques such as for airpath component identification. The device may include a pressure generator configured to generate a supply of pressurized air from an outlet along an air circuit to a patient interface. The device may include a sensor configured to generate a sound signal representing a sound in the air circuit. The device may include a dampening structure configured to reduce reflection of sound from the flow generator along the air circuit. The processor, such as of a controller, may be configured to process the sound signal so as to identify the patient interface and/or the air circuit. The processing may detect and combine acoustic signatures, such as by alignment and averaging, and/or may flatten a spectrum of the sound signal.