A fluid mixing device for mixing a first injection fluid and a second injection fluid includes a first fluid inlet, a second fluid inlet, a mixing chamber in fluid communication with the first and second fluid inlets, and an outlet port in fluid communication with the mixing chamber. The first fluid inlet is configured to conduct the first injection fluid in a first direction and has a first redirecting surface. The second fluid inlet is configured to conduct the second injection fluid in a second direction along a different axis from the first direction and has a second redirecting surface. The mixing chamber is configured to mix the first injection fluid and the second fluid together. The mixture of the first injection fluid and the second injection fluid exits the fluid mixing device via the outlet port.

A fluid handling cassette, such as that useable with an automated peritoneal dialysis (APD) cycler device or other infusion apparatus, may include a generally planar body having at least one pump chamber formed as a depression in a first side of the body and a plurality of flowpaths for a fluid that includes a channel. A patient line port may be arranged for connection to a patient line and be in fluid communication with the at least one pump chamber via at least a first one of said flowpaths, and an optional membrane may be attached to the first side of the body over the at least one pump chamber. In one embodiment, the membrane may have a pump chamber portion with an unstressed shape that generally conforms to the depression of the at least one pump chamber in the body and is arranged to be movable for movement of the fluid in a useable space of the at least one pump chamber. One or more spacers may be provided in the at least one pump chamber to prevent the membrane from contacting an inner wall of the at least one pump chamber. The patient line, a drain line, and/or a heater bag line may be positioned to be separately occludable in relation to one or more solution lines that are connectable to the cassette.

A system for enhanced sealing of coupled medical lines includes a male fitting, a female fitting, and a flexible annular collar seal. The seal provides a sealing function to an open end of the connector. The male fitting is made of medical grade materials and includes a male connector fluidly coupled to a first line. The female fitting is made of medical grade materials and including a female connector fluidly coupled to a second line and configured to mate with the male connector. The seal is made of a medical grade polymer coupled to one or both the male fitting and the female fitting.

The invention relates to a device for connecting multi-lumen lines for the medical field, in particular for wound care in the field of vacuum therapy, having a preferably one-piece basic body, designed for tight and preferably releasable connection of at least two line lumens, wherein the basic body, for furnishing a distributor chamber for at least one, preferably two, three, or more lumens, opening into it, of the connected line and preferably at least one channel for removing a fluid from and introducing it into the distributor chamber, and when the line is connected, the distributor chamber is sealed off in fluid-tight fashion from at least one line lumen in such a way that a fluid exchange between the distributor chamber and this line lumen is prevented.

Delivery systems and methods for forming and delivering biomaterials from two components are described herein. In particular, apparatus and methods for performing controlled delivery of multicomponent delivery of biomaterials into or onto a body part, such as a body lumen are described. More specifically, in some embodiments, the apparatus and methods are directed towards controlled delivery of micro-volumes of biomaterials into or onto a target location, the micro-volumes being defined as 0.001 mL-1 mL (or 1 μL-1,000 μL) of volume.

A medical connector that allows ventilation of vapor used in vapor sterilization and has an internal flow route that is tightly closable without using any separate clamping device. A medical connector includes a body having an internal flow route connected to an other flow route, proximal portions included in the body and having respective one-side connection ports at which the internal flow route is connectable to the one flow route, a distal portion having an other-side connection port at which the internal flow route is connectable to the other flow route, one-side lid portion, and an other-side lid portion whose state is switchable between a closing state and a ventilating state in which the other-side lid portion covers the other-side connection port such that ventilation is allowed.

A slip luer assembly includes a hub member and a latch member coupled to the hub member. The hub member includes an outer hub surface, an inner hub surface and a window surface. The window surface defines a window extending from the outer hub surface to the inner hub surface. The latch member includes at least one blade. The latch member is configured to be actuated between a first position and a second position. In the first position, the at least one blade is not positioned within the window of the hub member. In the second position, the at least one blade is positioned at least partially within the window of the hub member.

An apparatus, system and method of controlling the flow rate of an irrigation fluid. The apparatus, system and method include modifying a pressure gravitationally above the irrigation fluid in a fluid reservoir to increase the flow rate through a surgical pack by iteratively controlling infusion of gas to the fluid reservoir. The iteratively controlling comprises sensing an in-range response to said modifying, wherein the infusion of gas is enabled; and sensing an out-of-range response to said modifying. If, based on prior ones of said modifying: the out-of-range response poses no danger to a patient, the infusion of gas is enabled; the out-of-range response poses a substantial danger to the patient, the infusion of gas is disabled; or the out-of-range response poses no substantial danger to the patient, the iteratively controlling comprises applying a successive series of modifications to correct the out-of-range response.

A fluid connection assembly that includes a plurality of tubes having a first open end and a second open end opposite the first open end and a plurality of connectors. Each of the connectors include at least two connector portions, in which each of the at least two connector portions extend from a center of the connector and have a first end connected to the center of the connector and a second end connected to the second open end of one of the plurality of tubes. The connector portions are continuously formed with the tube and the center of the connector and the connector portions are fluidly connected together.

A system includes a tubing set and a drive assembly. The tubing set includes inlet tubing couplable to a source of fluid, a valve coupled to the inlet tubing, a syringe coupled to the inlet tubing via the valve, and outlet tubing coupled to the valve. The valve is configured to allow fluid to be drawn from the source of fluid via the inlet tubing into a syringe body of the syringe and to be expelled from the syringe body and through the outlet tubing, and to prevent fluid from being drawn from the outlet tubing into the syringe body and to prevent fluid expelled from the syringe body from flowing through the inlet tubing. The drive assembly is configured to reversibly receive the tubing set such that a drive mechanism is engaged with a plunger of the syringe to reciprocally translate the plunger relative to the syringe body.