An apparatus for rinsing sinuses or eyes, comprising a hand crushable container containing saline solution, and a dispenser configured to make a liquid tight seal with the container at one end, and a liquid tight seal with a nostril or an eye socket at the other end.

The present disclosure relates to an insert piece for a blood tubing set. The insert piece includes at least a first connection site for connecting a first tubing portion of the blood tubing set to the insert piece, and a second connection site for connecting a second tubing portion of the blood tubing set to the insert piece. The insert piece also includes a third connection site for connecting a third tubing portion of the blood tubing set to the insert piece, and a main line for forwarding a first liquid through the insert piece. The main line is in fluid communication with the first connection site and with the second connection site. The insert piece also includes a secondary line for forwarding a second liquid into the main line. The secondary line is in fluid communication with the third connection site.

An injection setup kit can include a manifold connector, a first packaging container, and a fluid line. The first packaging container can define a first closed interior volume that includes a patient interface connector having a patient interface inlet, a first patient interface outlet, and a valve configured to selectively permit fluid communication through the patient interface connector. The patient interface inlet can be fluidly connected to the manifold outlet. The fluid line can have a first fluid line end and a second fluid line end. The first fluid line end can be connected to the patient interface inlet within the first closed interior volume. The second fluid line end can extend outside of the first closed interior volume and be connected to a manifold outlet outside of the first closed interior volume.

A device for reconstituting a bioactive agent and forming a flowable paste is described. The device comprises a base configured for receiving: a first container containing a liquid, and a second container containing the bioactive agent, a syringe containing a paste forming material, the syringe being attachable to the base, wherein the base has a first conduit for fluidly connecting the first container with the second container and a second conduit for fluidly connecting the second container with the syringe, and wherein the first container is configured to be pressurizable such that when the first and second containers are received at the base, the liquid is forced through the first conduit into the second container, thereby reconstituting the bioactive agent, and the reconstituted bioactive agent is forced through the second conduit into the syringe, such that a paste is formed.

A medical connector coupling assisting tool for use with a lock connector part interconnecting at least two medical connectors, each of which includes a construction part, includes: at least two insertion parts configured to be inserted into respective portions defined by the constriction parts such that the insertion parts are thereby detachably mounted on the constriction parts; and a coupling part formed integrally with the at least two insertion parts and coupling the insertion parts together.

A tubing assembly for use with a fluid delivery system has a first fluid line having a distal end and a proximal end for connecting to a first fluid source, and a second fluid line having a distal end and a proximal end for connecting to a second fluid source. The tubing assembly further has a third fluid line having a distal end and a proximal end, and a connector assembly for connecting the distal end of the first fluid line and the distal end of the second fluid line to the proximal end of the third fluid line. A tubing holder receives at least a portion of the third fluid line. The tubing holder has a first portion and a second portion movable relative to the first portion to selectively block fluid flow through the third fluid line.

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.

A female syringe barrel is disclosed, which includes two protrusions provided on a cylindrical portion. A length (Lp) of each protrusion of the two protrusions along a direction, perpendicular to an axis of the cylindrical portion and perpendicular to a direction in which each protrusion of the two protrusions protrudes from the cylindrical portion, is 2.0 mm to 4.5 mm. A width of each protrusion of the two protrusions along an axial direction of the cylindrical portion is 1.0 mm to 2.1 mm. Each protrusion of the two protrusions has an inclined surface, which opposes a trailing flank of a screw when the two protrusions are engaged into the screw of a lock adapter, in an end portion close to a barrel body.

Automated injection system disclosed in this application advantageously provides physicians with a simplified interface for selecting fluid sources, such as saline, contrast, or a mixture of both, to inject at high pressures. The injector system may comprise a multi-use subassembly, a single-use subassembly, a fitting to fluidly connect the multi-use and single-use subassemblies, a hand held controller, a user interface, and an injector housing.

A membrane for a closed system transfer device including a material having 40-50% styrenic block copolymer, 0-10% polypropylene, and 45-60% by weight of mineral oil. The membrane may be utilized in any component of a closed system transfer device or system, such as a syringe adapter, patient connector, vial adapter, IV bag spike, etc. The membrane may also be utilized in scenarios where the cannula of the syringe adapter punctures the membrane and remains in the punctured position for an extended period of time, such as one hour or greater.