A method of dispensing a therapeutic fluid from a line includes providing an inlet line connectable to an upstream fluid source. The inlet line is in downstream fluid communication with a pumping chamber. The pumping chamber has a pump outlet. The method also includes actuating a force application assembly so as to restrict retrograde flow of fluid through the inlet while pressurizing the pumping chamber to urge flow through the pump outlet. A corresponding system employs the method.

A device configured to administer a medication can comprise a lower housing that includes a housing latch. The device can further comprise a needle guard that is movable relative to the lower housing along a first direction from a first position to a second position so as to expose a needle, and an upper housing supported relative to the lower housing. The upper housing can be configured to move with respect to the lower housing along a second direction from a pre-use position to a dispensed position. The housing latch can releasably interfere with the upper housing when the upper housing is in the pre-use position so as to prevent the upper housing from moving toward the dispensed position, and the movement of the needle guard toward the second position, causes the interference to be removed, thereby allowing the upper housing to move toward the second position.

A closure assembly for a medical device, preferably in the form of a tamper evident closure, having an outer sleeve including an open end and a closed end. A tip cap includes a flow restrictor disposed within the sleeve in accessible relation by the medical device through the open end. An indicator member is removably connected to the tip cap within the sleeve and a retainer member is connected to an interior of the sleeve in an interruptive, disconnecting relation to the indicator member by a snap-fit connection. The indicator member is captured within said hollow interior upon removal of said tip cap from the sleeve through the open end. An end cap may be attached to the sleeve, to define a closed end thereof, by a snap-fit connection similar to, but distinguishable from, the snap-fit connection between the retainer member and the interior of the sleeve.

A container holder assembly for a medicament delivery device is provided having a container holder and a needle assembly, where the container holder has a distal tubular body for receiving a multi-chamber container therein, the distal tubular body comprising a distal body engaging structure on an external surface configured to movably engage an actuator device of the medicament delivery device in order to releasably connect the container holder to the actuator device, and a proximal tubular part having a proximal body engaging structure connected to the needle assembly, where the needle assembly has a hub having an injection needle with a distal needle end and a proximal needle end, the distal needle end being isolated from the multi-chamber container when the multi-chamber container is received in the distal tubular body. A medicament delivery device having a container holder assembly is also provided.

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.

Devices, systems, and methods are provided herein for delivering medication (e.g., insulin) via a wearable pump having a patch-style form factor for adhesion to a user's body. The reusable pump may be coupled to a disposable cap housing a microdosing system for delivering precise, repeatable doses of medication to a cannula configured to deliver medication to a target infusion area beneath the user's outer skin layer. The system further may include an applicator for inserting the cannula into the user's skin and/or applying an adhesive pad to the skin.

A system for treating heart disease, such as pulmonary hypertension or right heart failure, including an implantable component and external components for monitoring the implantable component is provided. The implantable component may include a compliant member, e.g., balloon, coupled to a reservoir via a conduit. Preferably, the compliant member is adapted to be implanted in a pulmonary artery and the reservoir is adapted to be implanted subcutaneously. The external components may include a clinical controller component, monitoring software configured to run a clinician's computer, a patient monitoring device, and a mobile application configured to run on a patient's mobile device.

A disposable safety syringe needle and a syringe device including the same are provided, which can prevent reuse and an accident in safety, in which injury can be sustained by the needle. The disposable safety syringe needle includes: an upper part to which an elastic member is coupled and in which a needle member is inserted; a lower part which is coupled to one end of the upper part, and which includes one or more catching parts; and a safety part which is coupled to one end of the lower part, and which includes a catching protrusion, wherein the safety part is inserted into the lower part toward the upper part so that the elastic member is compressed, and the catching protrusion of the safety part is coupled to the one or more catching parts by the stretching force of the elastic member so as to disable reuse.

A sensor system capable of detecting tissue counter pressure from patients that utilize infusion pumps to administer their medication is provided. Embodiments include a retrofitted piece that is placed between the user's infusion set and pump, as well as a “smart” infusion set configured for measuring characteristics of a fluid traveling therethrough. Hardware is provided that couples with the sensor to store, analyze, and compare data to distinguish between normal and non-normal injection/infusion profiles. An alert system notifies the user of a malfunction within the pump, within the infusion set, or at the injection/infusion site.

A device adapted to provide evidence of tampering. The device comprises a sleeve and an insert that is positioned within the sleeve. The insert comprises a flap that is movable between a closed position and an open position. In particular, the flap is adapted to move from a closed position to an open position when the position of the sleeve relative to the insert is changed a predetermined amount to try to open the container. As a result, an open position of the flap would readily indicate tampering to a user. A system comprising a tray adapted to receive at least one said device is also provided.