A syringe assembly including: (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap holder assembly containing a cap and an absorbent material removably attached to the syringe.

Disclosed are systems that include a syringe having a barrel configured to hold a fluid and a plunger configured to draw the fluid into the barrel when the plunger is pulled backward through the barrel. The syringe is configured to inhibit forward movement of the plunger. For example, the systems can include mating pockets configured to engage barbs to inhibit forward movement of the plunger.

Syringe systems including barrels having lubricated portions and non-lubricated portions are provided. The non-lubricated portions may be configured to be loaded with injectable materials, such as embolic agents. The injectable materials may comprise polyvinyl alcohol. Also provided are plungers having plunger tips and seal members. Also provided are methods of lubricating portions of barrels of syringe systems with lubricants including silicone or silicone-free lubricants.

Devices used to deflate an inflatable hemostasis device are disclosed. The devices may be configured to deflate the inflatable hemostasis device in staged increments over a period of time. The devices may include a barrel member and a plunger member comprising an insert configured to couple with a retention ring of the barrel to restrict a retraction distance of the plunger member.

An antiseptic medical cap that may include a base, a sidewall, and a chamber configured to receive a proximal end of a medical fluid port having an opening. The antiseptic medical cap, in some instances, may include an insert having a gas-releasing anti-microbial compound and/or include a nitric oxide-releasing system that is configured to be positioned at least partially through the opening of the medical fluid port when the antiseptic medical cap receives the proximal end of the medical fluid port into the chamber.

A system includes a first cavity with an open upper proximal end and a distal end including a plurality of ports. A second cavity can be concentric with and advanceable through the open upper proximal end of the first cavity. The second cavity can include an open upper proximal end. A plunger can be on a distal end of the second cavity. The plunger can be configured to move a first constituent from the first cavity through at least one of the plurality of ports. A plunger rod can be advanceable through the open upper proximal end of the second cavity and configured to move a second constituent from the first cavity through at least one of the plurality of ports.

A medical syringe includes a ratchet for use during dispensing. The medical syringe, by virtue of the ratchet, enables repeated dispensing of a fixed amount of a relatively high-viscosity fluid to a target site within a patient. The medical syringe may be pre-filled with fluid and the fluid maybe sealed within the medical syringe. Accordingly, the medical syringe is configured to resist leaks and/or breaches that may occur as a result of manufacturing, sterilization, shipping, and/or storage.

A safety syringe comprising a needle redirection device that is desirably configured to bend the needle shaft forwardly of the barrel following an injection to thereby redirect the needle tip from a first position where it projects forwardly in coaxial alignment with the syringe barrel to a second position where the needle tip is covered or protected from incidental or accidental contact and associated needle sticks. Both sliding and pivoting embodiments are disclosed.

A liquid dispensing system for oral administration comprises a dispenser (16,18,20) and cartridges (14) from which medicine is dispensed. Each cartridge (14) includes a hollow shell (22,24) with a septum (26) at one end, a piston (28) at the other end, and the medicine in a cavity (23) between the septum and the piston. The dispenser includes receiver (20) in which a cartridge (14) is received, a plunger (18) that can slide relative to the receiver and that has a plunging head (52) that can drive the piston (28), and a barrel (16) in which the cartridge (14), receiver (20) and plunger (18) can be received, at least partly. Once a cartridge (14) has been inserted into the receiver (20), the receiver and cartridge are inserted into the barrel (16) and a piercing head (44) ruptures the septum (26). The plunger (18) is pushed to drive the piston (28) and the medicine is dispensed by the piston, through a discharge passage (42) of the barrel (16). The septum (26) can hinge on a hinge formation (86) to act as a one-way valve to prevent unintentional flow of liquid from the cartridge.

It is known that fluids, for example, drugs, may be administered via a syringe. It is further known that in some instances, a second fluid must be administered following the administration of a first fluid in order to flush the first fluid. There are numerous reasons for why such flushing may be required and/or desirable. For example, flushing ensures that a patient has received the entirety of a dose of the first fluid (e.g., a drug), that the first fluid does not mix and/or react with a subsequently administered (third) fluid that may be incompatible with the first fluid, and/or that the infusion lines are clean and/or primed for a subsequent infusion, to cite a few examples. The present invention is a novel syringe design that houses the flushing solution as part of the syringe to streamline the fluid delivery (drug) and the flushing solution subsequently.