A portable dual chamber auto-injector configured to store a dry opioid antagonist medicament separately from a liquid component, wherein a user actuated mixing system comprising a movable component to create a fluidic pathway between the first and second chambers and release a portion of energy from a pre-stored energy to drive a displacement mechanism into the first chamber and displace the liquid component into the second chamber and solubilize the opioid antagonist. A needle assembly in fluid communication with the second chamber can be used to transfer the solubilized opioid antagonist.

Systems and methods are disclosed for controlling the flow of fluids in a fluid infusion system. The system may include first and second fluid containers, first and second tubes coupled to the first and second fluid containers, and an external valve coupled to the second tube and configured to be attached to the first tube. The valve may be configured to shape the first tube to form a valve region which is opened or closed by an actuating element in the valve that is driven by hydrostatic pressure from the second tube. A full second container may generate a pressure that is concentrated through a diaphragm onto a pin which presses on the shaped first tube region, closing it to allow only fluid from the second container to flow. When the fluid level in the second line falls reducing pressure, the pin's force reduces until the first tube is opened.

Disclosed are methods of radioisotope infusion comprising infusing saline comprising a diagnostic dose of a radioisotope, and delivering a pre-measured volume of push saline. The disclosed methods confer improved image quality with low background noise, higher signal to noise ratio (SNR) and higher contrast to noise ratio (CNR), leading to better diagnosis and thus eliminating the need of repeating the infusion and imaging which in turn reduces exposure of a patient to radiation.

In some embodiments, a medical fluid connector is configured to receive an emitter of therapeutic agents to be emitted into a fluid pathway within the connector, the medical fluid connector comprising a proximal female end, an intermediate region, a distal male end, and a fluid pathway extending from the proximal female end, through the intermediate region, to the distal male end. A retaining structure is positioned within the intermediate region. The retaining structure is configured to securely receive an emitter of one or more therapeutic agents in a position and orientation where the fluid pathway is configured to convey fluid moving longitudinally through the fluid pathway directly into a proximal region of the emitter, around one or more lateral surfaces of the emitter, and toward the distal male end.

A device for administering an infusion or transfusion of liquid from a container includes a pump for pumping liquid to a patient connection via a conduit having a liquid-retaining filter membrane. The device also includes a pressure measuring device for acquiring measurement values corresponding to a pump-inlet-side pressure, and a control device for detecting a change in the pump-inlet-side pressure based on the measurement values. The control device determines, based on the change in the pump-inlet-side pressure, whether to stop pumping. The control device also generates a control signal when the pumping is to be stopped. Moreover, the control device emits, based on the control signal, a communication signal to a data connection between the device and a unit that reads the communication signal. In addition, or in the alternative, the control device switches the device from a first state to a second state based on the control signal.

Disclosed is a medical fluid connector configured to receive and dispense medical liquid. The medical connector can be structured to include an initial stage in which medical liquid is infused into the connector and dispensed out of the connector essentially unchanged. The medical connector also can be structured to include a subsequent stage in which medical liquid is not infused into the connector and a volume of therapeutic liquid is dispensed out of the connector. The therapeutic liquid can include a portion of the volume of the medical liquid that was infused into the connector in the initial stage plus a therapeutic additive.

An indicator includes a body having a first end, a second end opposite the first end, a first surface and a second surface opposite the first surface, each of which extends from the first end to the second end, and an aperture extending from the first end to the second end, the aperture being sized and shaped to receive a tube, and at least one of the first and second surfaces including a haptic signature formed thereon.

A method of administering subcutaneous treatment to a patient is provided. The method includes delivering, by a needle-free injection device, a first volume of a treatment at a first location on a surface of a body of the patient; detecting a movement of the needle-free injection device relative to the first location; determining, from the movement of the needle-free injection device relative to the first location, a second location of the needle-free injection device relative to the first location; determining a second volume of the treatment to deliver at the surface of the body of the patient at the second location; and delivering, by the needle-free injection device, the second volume of the treatment at the second location on the surface of the body of the patient.

An infusion pump drive and its methods of use are disclosed. In one embodiment, the infusion pump drive may include a transmission component and a spring in line with the transmission component. Displacing the transmission component may compress the spring to apply a force causing fluid to dispense from an associated reservoir. Depending on the particular embodiment, the transmission component may either be displaced continuously or displaced multiple times to dispense fluid from the reservoir.

A fluid injector system includes a powered fluid injector, a connection port configured to receive a single-use disposable set having tubing connected to a fluid inlet port at a first end and connected to a waste outlet port at a second end, and a detector associated with the connection port and configured to generate a signal in response to a sonic, infrasonic, or ultrasonic wave emitted from the single-use disposable set during a priming operation of the single-use disposable set. In some examples, the detector is configured to generate a signal if the frequency of the wave emitted from the single-use disposable set is outside a predetermined range of frequencies corresponding to a predetermined range of frequencies of air expelled from the tubing. A method for detecting the multiple uses of a single-use disposable set connected to a fluid injector system is also provided.