A medical device including an application device with a first fluid path and a container movably attached to the application device. The container and the application device have a second fluid path therethrough, the container includes an inner chamber that is intermediate proximal and distal portions of the second fluid path, the inner chamber is fluidly isolated from the proximal portion of the second fluid path at a first position of the container, and the inner chamber is fluidly coupled to the proximal and distal portions of the second fluid path at a second position of the container. The first fluid path bypasses the container and the passage of fluid through the first fluid path is separately controllable from the passage of fluid through the second fluid path.

This invention provides a means by which correct dosages of emergency medication can be provided to children under emergency situations. A color- and size-coded set of cylinders is provided where the colors match the color codes of the Broselow® Pediatric Emergency Tape, a common method by which the proper dosage for child is estimated based on the child's height. Each type of medication in the emergency kit has its own color-coded set of cylinders, such that once emergency medical personnel measure the child and determine which medication to use, all they need to do is grab the correct cylinder based on the color (which has already been determined from the Broselow® measurement). The invention allows emergency medical personnel to safely, efficiently, quickly, and accurately deliver the correct dosage of one or more medications to a child under emergency conditions.

Fluid transfer systems are disclosed that can be configured to transfer precise amounts of fluid from a source container to a target container. The fluid transfer system can have multiple fluid transfer stations for transferring fluids into multiple target containers or for combining different types of fluids into a single target container to form a mixture. The fluid transfer system can include a pump and a destination sensor, such as a weight sensor. The fluid transfer system can be configured to flush remaining fluid out of a connector to reduce waste, using air or a flushing fluid.

The invention relates to a needle interface (2) for connecting a hollow needle (3) having a proximal tip (3.1) to a medicament reservoir (1), the needle interface (2) comprising an inner ring (5) fixed to a reservoir wall (4) of the reservoir (1) and an outer ring (6) attachable to the needle (3), wherein one of the inner ring (5) and the outer ring (6) comprises at least one magnet (6.1) and wherein the other one of the inner ring (5) and the outer ring (6) comprises a magnetisable material (5.1) or a magnet (6.1).

A bag having two accesses, an inlet and an outlet, both containing closing devices for releasing or stopping the flow of a liquid that flows into or out of the bag. The inlet has a filtering element for retaining particles possibly produced by the coring phenomenon which can occur when the spike of the inlet ruptures the plug of the bottle. Also provided is a safety device used for permanently attaching the bottle to the inlet.

A dispenser comprises a cylinder in fluid communication with a one-way valve and an inlet in fluid communication with the cylinder. A lumen and a flow control member deliver fluid from a container to the inlet. A piston draws fluid through the flow control member and inlet into the cylinder upon movement of the piston in a first direction, and expels the fluid through the one-way valve upon movement of the piston in a second direction. The dispenser may be activated by either a “dual-action” mode of operation where an activating member is moved to retract the piston and provide the stored energy and then an-actuator is depressed to release the stored energy to the piston or a “single-action” mode of operation where an actuator is depressed in a single direction which concurrently retracts the piston, provides the stored energy and then releases the stored energy to piston.

A bioprocess vessel includes a flexible bag or substantially rigid container that defines an interior volume and having a bottom surface, the bottom surface being open or containing an aperture therein for the passage of fluid. A pump is secured to the bottom surface of the flexible bag or substantially rigid container. In some embodiments is secured directly to the flexible bag or substantially rigid container. In other embodiments, the pump is secured indirectly the flexible bag or substantially rigid container using, for example, a port that extends through the aperture on the bottom surface. The port or flanged surface may also be integrated into the pump, which is secured to the vessel. An optional mixing adaptor may be provided inside the interior volume of the flexible bag or substantially rigid container and at least partially covers the inlet that leads to the pump.

A dispensing mechanism includes at least two helical augers having threads, and at least two channels configured to hold the items to be dispensed. The items to be dispensed are received at least partially within the threads of the augers. The dispensing mechanism includes a drive mechanism engaged with the at least two augers and configured to rotate the at least two augers to transport the items to be dispensed, driven by the threads of the augers, to dispense the items from the dispensing mechanism. The dispensing mechanism may include a separable dispenser and cassette.

A method and apparatus for a connection interface between a reservoir or syringe, infusion set tubing, and an infusion pump is provided. The reservoir, a base and a cap are connected to form an integrated unit that is capable of being inserted and secured in an infusion pump housing. The cap and the infusion pump are each provided with at least one sensor or at least one detectable feature, arranged to interact with at least one corresponding detectable feature or sensor on the other of the cap and infusion pump device, to detect one or more of the presence, position or other characteristic of the cap when the cap is aligned or coupled with the infusion pump housing. The detectable feature and sensor may be magnetic, RF, mechanical, optical or any combination.

A drug vial safety device, including a cover that is securable to a drug vial is disclosed. The cover at least partially encloses at least a neck and a lid of the drug vial. The cover includes a port having a shape that restricts syringe access to the vial through the port to a syringe shaped to be compatible with the port shape.