A method of using a power-injectable port includes obtaining the power-injectable access port, attaching a catheter to an outlet stem of the power-injectable access port, and implanting the power-injectable access port and the catheter into a patient. The method further includes identifying the power-injectable access port following the implanting, and in accordance with the identification, inserting a distal end of a needle through the septum and into the reservoir, and injecting contrast media through the needle at a rate of at least one milliliter per second. The power-injectable access port includes a housing, a septum, a reservoir, and an outlet stem in fluid communication with the reservoir. The power-injectable access port is rated for injection of contrast media at a flow rate of at least 1 milliliter per second. The power-injectable access port is structured for operation at a pressure in the reservoir of at least 35 psi.

A method of performing a power injection procedure, including taking an x-ray of a subcutaneously implanted access port in a patient to determine whether the access port includes a radiographic feature indicating that the access port is suitable for flowing fluid at a rate of at least about 1 milliliter per second through the access port. The access port defines one or more fluid reservoirs, each fluid reservoir accessible through a cannula-penetrable septum. The method further includes identifying the indicating radiographic feature on the x-ray, and in accordance with the presence of the indicating feature on the x-ray, flowing a fluid through the access port at a rate of at least about 1 milliliter per second.

A connector includes an elastic valve body that includes a top face on which a slit is formed and a bottom face opposite the top face; and a holding section that is in contact with the top face and the bottom face of the elastic valve body and holds the elastic valve body. The holding section surrounds the slit, and the elastic valve body includes a peripheral section that is positioned outward of a portion of the elastic valve body that is held by the holding section. The elastic valve body and the holding section are configured such that a volume of the peripheral section in a state in which the elastic valve body is held by the holding section is larger than a volume of the peripheral section in a state in which the elastic valve body is not held by the holding section.

A method of using a power-injectable port includes obtaining the power-injectable access port, attaching a catheter to an outlet stem of the power-injectable access port, and implanting the power-injectable access port and the catheter into a patient. The method further includes identifying the power-injectable access port following the implanting, inserting a distal end of a needle through the septum and into the reservoir, and injecting contrast media through the needle at a rate of at least one milliliter per second. The power-injectable access port includes a housing, a septum, a reservoir, and an outlet stem in fluid communication with the reservoir. The power-injectable access port is rated for injection of contrast media at a flow rate of at least 1 milliliter per second. The power-injectable access port is structured for operation at a pressure in the reservoir of at least 35 psi.

A method of performing a power injection procedure, including taking an x-ray of a subcutaneously implanted access port in a patient to determine whether the access port includes a radiographic feature indicating that the access port is suitable for flowing fluid at a rate of at least about 1 milliliter per second through the access port. The access port defines one or more fluid reservoirs, each fluid reservoir accessible through a cannula-penetrable septum. The method further includes identifying the indicating radiographic feature on the x-ray, and in accordance with the presence of the indicating feature on the x-ray, flowing a fluid through the access port at a rate of at least about 1 milliliter per second.

A liquid injection port including a liquid input block defining a liquid input conduit; a compression block adapted to mate with the liquid input block; and a septum including a deformable material mounted in a septum retainer, the septum defining a central perforation, and forming a seal between the liquid input block and the compression block. The septum defines a conical deformation toward the liquid input conduit. A method for delivering fluid from a pipette tip includes a) introducing the fluid into the pipette tip; b) inserting the pipette tip into a pipette conduit defined by a compression block; c) inserting the pipette tip through a septum mounted in the compression block; and d) releasing the fluid in the pipette tip into a liquid input conduit defined in a liquid input block, the septum defining a conical deformation toward the liquid input conduit while maintaining a seal.

A medical connector for use in a fluid pathway includes a substantially transparent housing having a proximal end with a proximal opening and a distal end with a distal opening, and a cavity extending therebetween. The connector provides a substantially visible fluid flow path extending through a substantial portion of the connector.

A coupling system for a closed fluid transfer system includes a coupling member that features a coupling member housing. The coupling member housing includes a housing portion that at least partially surrounds a sealing member receptacle in an axial direction with respect to the longitudinal axis and which includes a coupling member housing threaded portion on the inner surface facing the sealing member. The coupling system also includes a mating coupling member for coupling with the coupling member. The mating coupling member includes a mating coupling member housing that has a mating coupling member guiding structure. The coupling member housing threaded portion of the coupling member is configured such that the mating coupling member guiding structure and the sealing member receptacle structure are jointly and movably guided, in particular in a predetermined positional relation to each other, by the coupling member housing threaded portion.

A Y-connector for medical lines, includes a tubular body provided with a first inlet coaxial to the tubular body and containing a valve device formed by an elastic element, and a second inlet arranged obliquely to the tubular body and communicating therewith between the first inlet and the outlet. The tubular body is formed with an inner septum for deviating a flow coming from the second inlet towards the hollow elastic element prior to directing the flow to the outlet.

An access port includes an access port body and a needle-penetrable septum. The access port body can be of integral single-piece construction, and can define a reservoir aligned with an access opening. The access port body can further define an annular groove between the reservoir and the opening. The annular groove can have a diameter greater than a diameter of the access opening and a diameter of the reservoir. The needle-penetrable septum can include an upper portion disposed in the access opening and an annular flange disposed in the annular groove. The annular flange can extend radially outward from a lower portion of the septum, and can have a diameter greater than a diameter of the upper portion of the septum. The needle-penetrable septum can further include an annular reinforcement structure disposed within the annular flange.