An introducer sheath is disclosed, which includes a tube body that is percutaneously inserted into a body lumen; and a hub that is connected to a proximal portion of the tube body. The tube body contains a polyvinylidene fluoride resin, a ratio of a thickness to an inner diameter of the tube body is 1/16 or lower, and a ration of a kink radius to an outer diameter of the tube body is 9.5 or lower.

A pumping system comprising a pump comprising a door for access within a housing of the pump, a pump segment configured for conveying a fluid based on compression of the pump segment, a pump segment frame for preventing said pump segment from stretching, a visual placement indicator configured for facilitating in a proper placement of the pump segment frame in the housing, and a non-pinching valve configured to be disposed in the housing and to control a flow of the fluid without requiring pinching of a tube.

Intravascular delivery system is designed for a safe and efficient access to secondary and tertiary vascular structures, such as the branches of the coronary sinus, to enhance the delivery and deployment of various catheters, such as, for example, pacemaker electrical leads. The over-the-wire system features a straight, or alternatively shaped, micro-catheter distal tip of an inner catheter that seamlessly cooperates with a peel-away reinforced outer catheter. The inner catheter and the peel-away reinforced outer catheter are advanced in their engaged mode of operation towards (or beyond) the target site. Subsequently, the inner and outer catheters are disengaged, and the inner catheter is removed from the outer catheter. A pacemaker lead may be advanced over the wire inside the outer catheter to the target site for deployment. Subsequently, the outer catheter is easily split and may be rapidly removed from the blood vessel.

An all-purpose drainage catheter which includes an all-purpose drainage catheter lumen, an extension tubing, a collection bag, a catheter hub, a Luer valve. The extension tubing inserted into the all-purpose drainage catheter lumen. The collection bag is fluidly coupled to the extension tubing. The Luer valve facilitates nephrostomy care so that when the all-purpose drainage catheter is in place urine flows from the renal pelvis into the all-purpose drainage catheter lumen, the extension tubing and the collection bag. The Luer valve employs a scalloped Luer-style male connector which, when screwed into the catheter hub, further allows urine to flow from the renal pelvis into the all-purpose drainage catheter lumen, the extension tubing and the collection bag. The all-purpose drainage catheter includes an outer catheter hub, an inner catheter hub coupled to the Luer valve at one end thereof and insertedly coupled to the outer catheter hub. A gear rack has a set of ratchet teeth and is disposed on and coupled to the inner catheter hub. A ratchet pawl disposed on and coupled to the outer catheter hub and aligned with the gear rack so that the ratchet pawl engages one of the ratchet teeth to secure the inner catheter hup to the outer catheter hub.

A medical female connector (10) for controlling a fluid flow is disclosed, as well as a method for its manufacturing, and medical devices including such a female connector. A tubular plunger (40) and a flexible valve member (60) are inserted into a housing (20). A distal end (42) of the plunger (40) is located at a distance proximally from the distal end (22) of the housing (20). In a flow stop configuration, the flexible valve member (60) seals a flow path (44) through the tubular plunger (40). In a flow configuration, the valve member (60) is compressed by a male connector (90) and deformed by the plunger (40) to allow a fluid flow through the plunger (40). A frusto-conical female sealing surface (24) is arranged to form a seal with the male connector (90). An entrance opening (25) of the housing (20) presents a diameter equal to or larger than the maximum diameter (d1) of the female sealing surface (24).

A guidewire support accessory includes one or more hollow tubular sections, each of the hollow tubular sections including a first end and an opposing second end for individually supporting a plurality of medical guidewires. A connector is disposed at the first end. Each of the one or more hollow tubular sections is sized and configured to receive a medical guidewire maintained in a coiled arrangement. The accessory includes at least one clamp configured to releasably retain a guidewire in the coiled arrangement, as well as at least one wiping or cleaning feature.

A system suitable for delivering a therapeutic agent to a target site may include a container for holding a therapeutic agent, a pressure source having pressurized fluid, where the pressure source is in selective fluid communication with at least a portion of the container, a catheter in selective fluid communication with the container and configured for delivery of the therapeutic agent to a target site, a first valve connected between the container and the catheter, a second valve connected between the pressure source and the container, a button configured to selectively actuate the second valve, and a brake assembly coupled to the first valve and configured to selectively permit actuation of the second valve, such that when the first valve is in a first state, the brake assembly blocks the button such that the button does not actuate the second valve.

Various embodiments of an antimicrobial insert for a stopcock medical connector are provided. More specifically, the present invention relates to an antimicrobial insert that is seated within at least a portion of the annular bore of the connector's tap, wherein fluid within the annular bore contacts the antimicrobial insert, thereby preventing microbial proliferation within the stopcock medical connector.

A medical fluid coupling for connecting a fluid line to a connection section of a blood treatment apparatus or for connecting to a connecting adapter comprises at least one main body. The main body includes a first latching element with a first section. The first section is designed to be elastically bendable and/or elastically tiltable. The main body may optionally include a second latching element with a second section. At least one of the first latching element and the second latching element comprises a recess for receiving a protrusion of the connection section and/or a protrusion to reach into a recess of the blood treatment apparatus or of the connecting adapter.

A three-way urology catheter stopcock includes a stopcock body defining a longitudinally extending fluid flow passage, the body having three connector mounting openings in a wall thereof, an on/off selector movably mounted within the fluid flow passage of the body, the on/off selector including a longitudinally extending, cylindrical selector body having an open end, a closed end, and three fluid flow openings in a wall of the selector body, wherein the closed second end includes one of a plurality of fluid flow indicator members and fluid flow indicia, two first connectors mounted in opposing connector mounting openings of the stopcock body, and a second connector mounted in the connector mounting opening that is between the openings in which the two first connectors are mounted.