Abstract: An IV infusion set includes at least one infusion component, a first IV tube coupled to the infusion component, a second IV tube and a disposable pump head that. The pump head includes an inlet port coupled to the first IV tube, an outlet port coupled to the second IV tube and a drive interface configured to be coupled to a first end of a drive shaft. The drive interface is configured to be rotated by rotation of the drive shaft having a second end coupled to a driver to increase a fluid flow rate through the IV infusion set. IV set assemblies and methods of use are also provided.

Abstract: Activatable medicament delivery containers and assemblies are disclosed that can be activated to direct a medicament from the container using an expandable material that causes an expansion chamber to displace the medicament from the container, where the medicament can be directed from the container at a predetermined or use-specific rate, and for a predetermined period of time, and the container being couplable with a dock to form an activatable medicament delivery assembly, where the container can be removably coupled or replace with the dock, and where the dock can be coupled directly to an intravenous fluid delivery device.

Abstract: A fluid-fitting tool is disclosed that can align with and rotationally couple with a fluid fitting where the fluid-fitting tool can include a passage and an engagement feature for engaging against the fluid fitting such that when the fluid-fitting tool is spaced apart from the fluid fitting, the fluid-fitting tool can move in a longitudinal direction toward and away from the fluid fitting, and can rotate relative to the fluid fitting around a longitudinal axis of the passage, and when a portion of the fluid-fitting tool and the fluid fitting are rotationally aligned and longitudinally overlap, the fluid-fitting tool can move longitudinally relative to the fluid fitting, and the fluid fitting is rotated when the fluid-fitting tool is rotated around a longitudinal axis of the passage.

Abstract: Anti-microbial compositions for cleaning and sanitizing skin are disclosed. The anti-microbial compositions preferably comprises at least one quaternary ammonium chloride active and results in low irritation cleansing and sanitizing products that allow more frequent application.

Abstract: A pressure detection system includes a body having an internal chamber with input and output ports and a flexible membrane fluidically sealed to an exposed opening of the chamber to prevent a fluid passing through the chamber from passing through the exposed opening. The membrane is configured to change shape responsive to an increase in pressure caused by the fluid within the chamber satisfying a predetermined threshold. In some implementations, the membrane includes or is part of an identification mechanism which moves outwards, away from the chamber, as the pressure increases to indicate the pressure increase. In some implementations, the identification mechanism includes markings on the surface of the membrane, and an image sensing device reads the markings, and provides an indication of a current pressure associated with the fluid in the chamber based on a variation in the markings from a default state.

Abstract: Medical fluid extension set systems are disclosed that can include a tubing anchor coupled to tubing and a fluid coupling device, and can be anchored to a patient to resist unintended separation of the tubing anchor or a catheter coupled to the tubing, from a patient, and to permit separation or disconnection of a fluid pathway between the tubing and another device coupled to thereto upon exceeding a pulling force on the fluid coupling device, and where disconnection includes separation of first and second valve assemblies such that a fluid pathway of the first and second valve assemblies is obstructed upon disconnection of the fluid coupling device.

Abstract: A disinfecting, sanitizing and cleaning composition is a formulation that is safe for use on food contact surfaces without the need for any post-application water rinse. In one exemplary embodiment, the cleaning and disinfecting composition eliminates the need for the post-application water rinse by using only components that are considered Food Safe by the EPA. In another exemplary embodiment, the cleaning and disinfecting composition the includes citric acid, but without any anionic surfactants in the cleaning and disinfecting composition. In still another exemplary embodiment of the disclosure, the cleaning and disinfecting composition includes a second organic acid and one or more nonionic surfactants as components along with citric acid to provide unexpected and beneficial antimicrobial properties to the cleaning and disinfecting composition.

Abstract: A male luer connector is provided that includes a luer slip having a first material, the luer slip sized and shaped to mate with a female connector. A collar is disposed on an outer surface of the luer slip, the collar having a second material and a plurality of first grip features disposed on an outer surface of the collar. A grip is coupled to the luer slip, the grip having a third material and a plurality of second grip features disposed on an outer surface of the grip, wherein one of the plurality of first and second grip features are configured to provide a slip resistant grip surface. Infusion sets and infusion set luer connector assemblies are also provided.

Abstract: A dual-chamber syringe may include an end wall and a primary plunger. The primary plunger may include a primary stopper. The primary stopper may form a primary chamber with the end wall. A secondary plunger may be in mechanical association with the primary plunger. The secondary plunger may include a secondary stopper. The secondary stopper may form a secondary chamber with the primary stopper. A primary nozzle may extend from the end wall and may be in fluid communication with the primary chamber. A secondary nozzle may extend from the end wall and may be in fluid communication with the secondary chamber.

Abstract: A medical connector may include a body having an outer surface and an inner surface defining a lumen of the body, an inlet port defined at a proximal end of the body, and an outlet port defined at a distal end of the body. The medical connector may further include a compressible valve member comprising a normally closed slit and disposed in the lumen and extending through the inner and outer surfaces of the body to an exterior of the medical connector. The compressible valve member may be configured to compress radially inward to open the slit upon insertion of the body into a medical access device, and expand radially outward to close the slit upon disconnection of the body from the medical access device.

Abstract: A dual-chamber syringe may include an end wall and a primary plunger. The primary plunger may include a primary stopper. The primary stopper may form a primary chamber with the end wall. A secondary plunger may be in mechanical association with the primary plunger. The secondary plunger may include a secondary stopper. The secondary stopper may form a secondary chamber with the primary stopper. A primary nozzle may extend from the end wall and may be in fluid communication with the primary chamber. A secondary nozzle may extend from the end wall and may be in fluid communication with the secondary chamber.

Abstract: An exemplary syringe adapter for coupling with a syringe may include a housing. A needle-free connector may be disposed in the housing. A communication member may be in slidable engagement with the housing. The communication member may be slidable, with respect to the housing, between an unactuated state and an actuated state of the syringe adapter. A cannula may extend from the communication. In the unactuated state, the cannula may be retracted within the needle-free connector. In the actuated state, the cannula may protrude through and axially beyond the needle-free connector.

Abstract: An exemplary syringe adapter for coupling with a syringe may include a housing. A needle-free connector may be disposed in the housing. A communication member may be in slidable engagement with the housing. The communication member may be slidable, with respect to the housing, between an unactuated state and an actuated state of the syringe adapter. A cannula may extend from the communication. In the unactuated state, the cannula may be retracted within the needle-free connector. In the actuated state, the cannula may protrude through and axially beyond the needle-free connector.

Abstract: Bulbs for use with an IV set are described herein. A bulb includes a bulb body and a filter. The bulb body defines an inlet, an outlet, and a bulb volume in fluid communication with the inlet and the outlet. The filter is in fluid communication with the bulb volume. The filter captures particulate from a flow from the inlet to the outlet. The bulb body is deformable to compress the bulb volume and direct back flow from the bulb volume through the filter, agitating particulate captured in the filter, unclogging the filter and allowing for more flow.

Abstract: Drip chamber assemblies are described herein. A drip chamber assembly includes a drip chamber and a filter. The drip chamber includes a chamber body defining a chamber volume. The filter is disposed within the chamber volume. The filter includes a folded filter media, which defines an inlet portion of the chamber volume and an outlet portion of the chamber volume. The folded filter media permits inlet flow from the inlet portion of the chamber volume to the outlet portion of the chamber volume. The folded filter media captures particulate from the inlet flow.

Abstract: IV spikes are described herein. An IV spike includes a spike body. The spike body can be formed of a first material and can include a spike portion converging to a point. The IV spike further includes at least one spike flow port formed through the spike body. The IV spike further includes a lower flow port in fluid communication with the at least one spike flow port. The IV spike can also include an overmolded engagement feature disposed around the spike body, wherein the overmolded engagement feature comprises a second material and is configured to retain the IV spike within an IV container.

Abstract: Anti-microbial compositions for cleaning and sanitizing skin are disclosed. The anti-microbial compositions preferably comprises at least one quaternary ammonium chloride active and results in low irritation cleansing and sanitizing products that allow more frequent application.

Abstract: Anti-microbial compositions for cleaning and sanitizing skin are disclosed. The anti-microbial compositions preferably comprises at least one quaternary ammonium chloride active and results in low irritation cleansing and sanitizing products that allow more frequent application.

Abstract: IV spikes are described herein. An IV spike includes a spike body. The spike body can be formed of a first material and can include a spike portion converging to a point. The IV spike further includes at least one spike flow port formed through the spike body. The IV spike further includes a lower flow port in fluid communication with the at least one spike flow port. The IV spike can also include an overmolded engagement feature disposed around the spike body, wherein the overmolded engagement feature comprises a second material and is configured to retain the IV spike within an IV container.

Abstract: Vented syringes are described herein. A vented syringe includes a syringe body and a plunger body. The syringe body defines a syringe cavity. The plunger body is at least partially disposed within the syringe cavity. The plunger body includes an air intake channel defined within the plunger body. The vented syringe further includes a plunger seal that is sealingly engaged with the syringe cavity to cooperatively define a syringe volume. The vented syringe further includes a one-way valve in fluid communication with the air intake channel and the syringe volume, wherein the one-way valve is configured to prevent fluid flow from the syringe volume to the air intake channel and permit fluid flow from the air intake channel to the syringe volume.