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.

The embodiments of the present application provide an information processing method and apparatus, wherein the method is applied to a first client side, including: receiving therapy data from a therapy device, wherein the therapy data carries therapeutic effect data, a device identification corresponding to the therapy device, and a therapy parameter; sending the therapy data; and receiving parameter update information corresponding to the therapy data, wherein the parameter update information carries a latest therapy parameter acquired by updating the therapy parameter according to the therapeutic effect data, and the device identification corresponding to the therapy device. The embodiments of the present application can collect the therapy data of a user in time and conveniently, and improves the collecting efficiency of the therapy data.

A dose control device adapted to be removably mounted onto an exterior peripheral surface of an injectable drug delivery device, the drug delivery device including a substantially elongate drug delivery body, at least one injectable drug held by the body, the body having a distal and proximal extremity. The dose control device includes a first component configured to fit and substantially encase at least a portion of an exterior peripheral surface of the drug delivery device, and located at a proximal extremity of the drug delivery device; a second component configured to fit and substantially encase a corresponding remaining unencased portion of the exterior peripheral surface of the drug delivery device, and also located at a proximal extremity of the drug delivery device. The first component and the second component removably engage with each other to form a unit having a longitudinal bore that extends along a longitudinal axis of the drug delivery device, and in which bore the drug delivery device is encased between the first component and the second component.

Various embodiments of a device, a kit and method for delivering a drug depot are disclosed. The device comprises a housing including a lower body, an upper body, a ring member; and a drug cartridge. The lower body defines a lower body channel. The upper body defines an upper body channel. The drug cartridge defines a depot channel. The ring member is disposed extending upward from an annular step surface of the lower body toward a housing upper end. The ring member includes indicia indicating a characteristic of one or more drug depots in the drug cartridge. A plunger has a push rod for expelling the drug depot through the cannula to a site in the patient. A kit comprises the above components. A method includes assembling the components including selecting a ring member having indicia corresponding to one or more drug depots in the drug cartridge.

A system for blood treatment can include a dialysis machine and an ultrasonic authentication device connected to the blood treatment machine, the ultrasonic authentication device configured to scan a label and send signals containing label information to the dialysis machine.

A mist inhaler device (200) for generating a mist for inhalation by a user. The device comprises a mist generator device (201) and a driver device (202). The driver device (202) is configured to drive the mist generator device (201) at an optimum frequency to maximise the efficiency of mist generation by the mist generator device (201).

A tip cap for a medical injection device, including: a tip connector configured to engage a tip of the medical injection device; a closure cap configured to sealingly close a distal opening of the tip, the closure cap being releasably connected to the tip connector; an RFID tag including a chip and an antenna, where the chip is overmolded in one of the tip connector and the closure cap and the antenna is overmolded in the other one of the tip connector and the closure cap, the chip and the antenna being electrically connected by a bridge configured to break under a relative movement applied to the closure cap and the tip connector in order to release the closure cap from the tip connector, and the antenna is located at an interface between the tip connector and the closure cap.

A test fixture for testing aerosol provision devices may include a housing, a plurality of testing modules disposed at the housing where each of the testing modules includes a cavity configured to receive a portion of an aerosol provision device, and processing circuitry operably coupled to the testing modules. Each of the testing modules may be configured to interface with an assembly of a respective one of the aerosol provision devices to transition the assembly between an initial state and a transitioned state during a functional test controlled by the processing circuitry. The processing circuitry may be configured to conduct the functional test of at least two of the testing modules simultaneously.

A case for an electronic cigarette vaporiser, the case including an automatic lifting mechanism that lifts the vaporiser up a few mm from the case to enable a user to easily grasp the vaporiser and withdraw it from the case. The lifting mechanism can be spring-based. The case both re-fills the vaporiser with liquid and also re-charges a battery in the vaporiser.

Systems and methods for reducing the burden of recharging on patients and caregivers are provided. The systems and methods use a microbe removal layer upstream of a sorbent cartridge in a sorbent-based dialysis system. The systems and methods can determine whether the bacterial content and remaining capacity of a non-recharged sorbent module are suitable for the sorbent module to be reused safely and effectively without recharging.