Provided is a method for delivering a medical fluid. The method includes delivering a fluid volume, which includes contrast and/or a flush fluid, at a preselected total volumetric flowrate during a first duration of a fluid delivery procedure. The amount of the contrast agent and the flush fluid in the fluid volume can be controllably varied during the first duration of the fluid delivery procedure so as to substantially maintain a preselected total volumetric flowrate throughout the first duration of the fluid delivery procedure. Also provided is a fluid delivery system capable of performing this method.

A system for purging air from a feeding line is set forth. The system includes a charging device configured to selectively provide an air charge in the system. A restricting tubing can be located between the charging device and a delivery tube. The restricting tubing can be configured to tunably limit the air charge delivered from the charging device to the feeding line through the delivery tube.

The instant invention discloses a low-profile infusion set for the infusion and aspiration of fluid. The infusion set comprises an infusion tubing, an extension tube, a housing, a needle, and a needle holder. The extension tube and needle are connected to the housing, creating improved fluid pressure rates and flow rates.

A syringe assembly includes (i) a syringe with a cylindrical body, luer tip at a first end, finger grip at a second end and a cannula extending from the luer tip into the cylindrical body, and (ii) a plunger unit having an adapter portion, receiving cavity, finger grip and piston. A channel extends the length of the adapter portion to receive the cannula in one end and a variety of connectors, valves and/or syringes in a second end. The end of the channel accessible in the receiving cavity mates with or engages any number of commercially available valves, connectors and/or syringes while the luer tip similarly connects to any number of valves, catheters, connectors, etc., depending on the task being undertaken with the syringe assembly.

Syringe assemblies are described herein. A syringe assembly includes an assembly housing, a first syringe, a second syringe, and a connecting gear. The first syringe is disposed within the assembly housing. Each plunger is movable within the respective syringe cavity and defines a respective chamber in the respective syringe cavity, wherein the respective chamber is in fluid communication with the respective syringe port, the respective plunger comprising a respective gear rack extending longitudinally along the respective plunger. The connecting gear is rotatably coupled to the assembly housing. The connecting gear is configured to be in meshed engagement with at least one of the first gear rack and the second gear rack of the syringes.

A therapeutic device for treating an acute medical condition of a patient such as cardiac arrest is provided. The device includes one or more sensors that monitor parameters such as heart rhythm that relate to the patient's medical condition. The device also includes a plurality of medication reservoirs, each reservoir including a conduit, wherein each reservoir holds a predetermined medication that may be used to treat the condition. A manifold is connected with the reservoirs via their respective conduits. A delivery line is connected with the manifold to deliver fluids from the manifold to the patient intravenously. One or more medication pumps are in fluid connection with respective ones of the reservoirs. A processor is connected with the sensors. The processor includes a memory that stores processing instructions to interpret the parameters and to determine a recommended medication to deliver to the patient based on the parameters, the recommended medication being one of the predetermined medications. The processor is operatively connected with the medication pumps. When a recommended medication is determined, the processor actuates the medication pump connected with the reservoir including the recommended medication to deliver the medication to the patient via the manifold and the delivery line.

A vascular access device adapter allowing for interchangeable connections between separate components of a larger extravascular system while minimizing exposure to non-sterile environments in point-of-care testing and analysis is provided. The vascular access device adapter includes a body having a self-healing puncturable septum secured by an end cap by which hollow small gauge needles may extract or deposit fluid. The adapter device further includes an end cap enclosing the septum, the end cap having ribs which removably secure the adapter to the inner housing of a sample collection device.

Feed and flush delivery devices are described for use in switching between delivery of enteral feeding fluid and flushing/hydration fluid to a patient, with both fluids being delivered through the same closed system. The delivery devices are simpler, easier to use, and are more cost effective than known prior art valves and control devices. Independent feed and flush lines are typically received by the delivery device, which merges the two lines into a single end delivery line so that either feeding or flushing fluid, but not both at the same time, can be conveyed through the end line, as desired and selected by the user. The delivery device is loaded onto the pumping mechanism of an enteral infusion pump, and can be part of a cassette which is used in combination with a particular brand of infusion pump.

An intravenous bag attachment for automatically flushing remnants out from an intravenous line after the contents of a connected intravenous bag have emptied out. The attachment includes a container having a tubular member in fluid communication with an interior volume designed to hold a flushing solution. The tubular member is designed to create an opening and be inserted into an intravenous bag, and to act as a float valve that will remain closed while the amount of liquid remaining in the intravenous bag is above a predefined threshold, and that will open once the amount of liquid remaining in the intravenous bag falls below the predefined threshold. The float valve further includes a ball float designed to keep the tubular member upright, such that the float valve is closed, and to allow the flushing solution to exit through the tubular member when the float valve is open.

Apparatus and methods of dispensing fluid intravenously to a subject, and of flushing a line of an intravenous fluid administration apparatus, are provided. The apparatus may include a reservoir pump configured to operate in fluid communication with an upstream source of a first fluid and a downstream pressure-operated valve. The apparatus may also include a port connector configured to operate in fluid communication with at least the pressure-operated valve. The reservoir pump may also be configured to, during operation, automatically refill itself with the first fluid from the first upstream source. The downstream pressure-operated valve may be configured to operate in fluid communication with the reservoir pump and a second fluid source upstream of the pressure-operated valve, and to, during operation, dispense the first fluid to tubing downstream of the pressure-operated valve based on a pressure condition within the pressure-operated valve exceeding a threshold pressure.