An obturator can include antimicrobial features which assist in sterilizing or maintaining the sterility of fluid contained within a vascular access device while the device is not being used for infusion or other access to the patient's vasculature. These antimicrobial features include antimicrobial coatings applied to various surfaces of an obturator and antimicrobial components bonded or otherwise secured to an obturator. Various combinations of antimicrobial coatings and/or components can be used on an obturator as necessary to provide a desired amount of antimicrobial agents within a particular enclosed volume of a vascular access device.

A catheter assembly includes: an inner needle; an inner needle hub connected to the inner needle; a catheter through which the inner needle is inserted; a catheter hub connected to a proximal end portion of the catheter; and a protector that covers at least the tip of the inner needle when the inner needle is withdrawn. The protector includes: an inner tube, and an outer tube. The inner tube includes at least one arm that releasably engages with a proximal end of the catheter hub. The catheter assembly is configured such that, when the inner needle is withdrawn, after the tip of the inner needle has been stored in the protector, the outer tube is retracted with respect to the inner tube thereby allowing the at least one arm to be displaced outwardly, whereby engagement between the at least one arm and the catheter hub is released.

A bladder catheter includes a tube, wherein the tube has an insertion section for inserting into a urinary bladder through a urethra and wherein the tube has a connection section for connecting connection elements, wherein fluid can be drained from the urethra at the connection section via the insertion section, wherein a closable valve is arranged between the insertion section and the connection section in such a way that the discharge of fluid from the connection section can be prevented while the valve is closed.

A patency system for maintaining a patency of an indwelling medical device including an elongated shaft configured to be at least partially received within a portion of the indwelling medical device, and at least one cleaner configured to at least partially dislodge debris formed within the indwelling medical device.

Double-lumen infusion catheter including: a shaft having proximal section, distal section, and intermediate section therebetween; first and second lumens extending along a length of the shaft and having arc shaped wall therebetween; and an inflatable member provided distally to intermediate section, and over the distal section. First lumen has cross section larger than cross section of second lumen and is configured to receive a guidewire therethrough and allow fluid flow via an unobstructed portion of first lumen. Unobstructed portion is formed along guidewire outer surface, between guidewire outer surface and inner wall of first lumen, and extends from an inlet at proximal end of intermediate section to an outlet at distal end of intermediate section. First lumen is narrowed to approximate a first diameter in shaft proximal and distal sections, and is widened to approximate a second diameter greater than first diameter in the shaft intermediate section.

A method of manufacturing a safety catheter includes providing a catheter having a catheter body comprising an exterior surface, a drainage lumen, and an inflation lumen, forming a balloon inflation port between the exterior surface and the inflation lumen, forming a deflation port between the exterior surface and one of the inflation and drainage lumens, fixing a balloon sleeve to the exterior surface over at least the balloon inflation port to define a fluid-tight balloon interior between an interior surface of the balloon sleeve and at least a portion of the exterior surface, removably inserting a deflation plug in the deflation port to water-tightly seal the deflation port until the deflation plug is removed, connecting a proximal portion of a deflation connector to an inside surface of one of the lumens, and connecting a distal portion of the deflation connector to the deflation plug.

A safety balloon catheter includes a catheter having a stretch valve, a connector, a balloon inflated with an inflation fluid, a hollow inflation lumen extending through the catheter to the balloon and conveying inflation fluid thereto and therefrom, a hollow second lumen, and a balloon drainage port fluidically connecting the balloon to the second lumen. The stretch valve has a hollow base fixed in the second lumen at a proximal catheter end and shaped to permit a fluid therethrough and a hollow plug slidably positioned in the second lumen at a given distance from the base to, in a steady state, prevent inflation fluid from passing through the drainage port and, when actuated, slide within the second lumen to permit inflation fluid to pass through the drainage port and into the second lumen. The connector connects the base and the plug and has a length greater than the given distance.

Techniques are described for a medical device that includes a securing balloon inside of a guide catheter. A catheter comprising a proximal portion, a distal portion, and an expanding member located at the distal portion, said distal portion having an inner wall and an outer wall, said expanding member attached to said distal portion at the inner wall.

Medical devices useful in the delivery of chemotherapeutic agents, kits and methods are described. An example catheter comprises an elongate member having an elongate member proximal end, an elongate member distal end, and an elongate member main body extending between the elongate member proximal end and the elongate member distal end. The elongate member main body defines an elongate member circumferential wall, first, second, and third openings on the elongate member proximal end, a first heating lumen extending from the first opening toward the elongate member distal end, a second heating lumen extending from the second opening toward the elongate member distal end, and a treatment lumen extending from the third opening toward the elongate member distal end. The treatment lumen comprises a blind passage. The elongate member circumferential wall defines a plurality of passageways providing fluid communication between the treatment lumen and an environment external to the catheter.

Double-lumen infusion catheter including: a shaft having proximal section, distal section, and intermediate section therebetween; first and second lumens extending along a length of the shaft and having arc shaped wall therebetween; and an inflatable member provided distally to intermediate section, and over the distal section. First lumen has cross section larger than cross section of second lumen and is configured to receive a guidewire therethrough and allow fluid flow via an unobstructed portion of first lumen. Unobstructed portion is formed along guidewire outer surface, between guidewire outer surface and inner wall of first lumen, and extends from an inlet at proximal end of intermediate section to an outlet at distal end of intermediate section. First lumen is narrowed to approximate a first diameter in shaft proximal and distal sections, and is widened to approximate a second diameter greater than first diameter in the shaft intermediate section.