A catheter assembly may include a catheter adapter, which may include a distal end, a proximal end, a lumen extending between the distal end and the proximal end, and a side port. A septum may be disposed within the lumen of the catheter assembly. The side port may include a lumen in fluid communication with the lumen of the catheter adapter. The lumen of the side port may be distally-facing, which may facilitate flushing of fluid trapped proximate a distal face of the septum. The catheter assembly may include a catheter secured within the catheter adapter and extending distally from the catheter adapter.

Disclosed is an angioplasty balloon catheter and method of use, said angioplasty balloon catheter includes an elongated tip end with physical characteristics nearly identical to a standard angiographic diagnostic catheter. The elongated tip end extends approximately between 2 cm to 75 cm beyond a distal end of a balloon, depending upon embodiments. The tip of the elongated tip end may be angled or straight depending upon embodiments and may or may not have a plurality of side holes in addition to an end hole depending on embodiments. The elongated tip end permits the angioplasty balloon catheter to tract more easily across tortuous or markedly angulated segments of a dialysis graft or fistula, minimizing complications that can result with currently available devices. If angulated, the elongated tip end also enables a user to selectively catheterize an artery without needing a separate diagnostic catheter to do so, and enable tracking and cornering across sharply angulated vessel segments. Whether with an angled or straight distal catheter portion, the angioplasty balloon catheter disclosed herein allows the user to perform angioplasty of an inflow segment of a dialysis graft or fistula and then perform post angioplasty angiographic imaging without the need to exchange the angioplasty balloon catheter for a diagnostic catheter, advance the balloon catheter into the native artery, or perform a blowback angiographic run, thereby improving safety and reducing procedure time.

A flow restriction device may include a proximal housing including an internal fluid channel, a distal housing including an internal fluid channel, and an intermediate housing interposed between the proximal and distal housings. The intermediate housing may include an internal chamber, and a slider reciprocally disposed in the internal chamber. The slider may include an internal fluid channel and a seal overlaying an outer surface of slider excluding the fluid channel, and may be reciprocally movable between (i) a first position where the internal fluid channel of the slider is axially aligned with the internal fluid channels of the proximal and distal housings to allow a fluid to flow therethrough, and (ii) a second position where the internal fluid channel of the slider is not aligned with the internal fluid channels of the proximal and distal housings and the seal blocks fluid connection between the proximal and distal housings.

A urethral catheter. A cavity is formed at the head end of the urethral catheter, and an internal span of the cavity is greater than that of an opening. A check device (2) located at the front end of a guide core (5) is received in the cavity, and the check device (2) is a guide core (5) that can be retracted into a guide core catheter (4) and can move within the guide core catheter (4). The guide core (5) can expand outward after moving out of the guide core catheter (4). The span of the top of the expanded guide core (5) is greater than the outer diameter of the opening of the cavity at the head end of the urethral catheter. The urethral catheter eliminates a guide extension inserted inside the urethral catheter, and avoids any structural parts provided in the front end of the urethral catheter, and no accessory device is provided at the inner side of the catheter wall of the conventional urethral catheter, so that the internal urination cross-sectional area of the urethral catheter is the same as the area of the inner holes of the urethral catheter, thereby greatly increasing the urine output of the urethral catheter and greatly reducing the injection resistance of a lubricant.

Devices and methods for management of a guidewire during catheter insertion. Particular embodiments include unidirectional valves to allow movement of a guidewire in one direction only.

A medical liquid injection device including a catheter with a hollow shaft having a lumen formed inside to contain medical liquid, a wire to be inserted into the lumen, and a wire moving device to move the wire forward inside the lumen from a proximal end to a distal end side in accordance with a control signal, thereby ejecting a predetermined amount of the medical liquid from the distal end of the hollow shaft.

Rapidly insertable central catheters (“RICCs”), RICC insertion assemblies, and methods are disclosed. For example, a RICC insertion assembly can include a RICC, an introducer, and an access guidewire. An introducer needle can include a needle shaft having a longitudinal gap extending from a proximal portion of the needle shaft through a needle tip. An introducer sheath can include a splittable sheath hub coupled to a splittable sheath body. The introducer sheath can be disposed over the introducer needle with the sheath body sealing the needle shaft for drawing a vacuum through the introducer needle. The access guidewire can extend along an entirety of a primary lumen of the RICC, through a splittable valved port of the sheath hub, along a sheath body-covered needle channel of the needle shaft, and to a location in the introducer proximal of the needle tip in a ready-to-operate state of the RICC insertion assembly.

A catheter assembly may include a catheter adapter, which may include a distal end, a proximal end, an inner surface extending through the distal end and the proximal end and forming a lumen, and a side port forming a side port pathway through a sidewall of the catheter adapter and in fluid communication with the lumen. The catheter assembly may include a catheter extending distally from the distal end of the catheter adapter. The catheter assembly may include a septum disposed within the lumen proximal to the side port pathway. A portion of the inner surface proximal to the catheter and distal to the septum may include one or more of the following: a textured surface, a channel configured to direct fluid flowing into the lumen from the side port, a protrusion extending inwardly into the lumen opposite the side port pathway, and an annular shoulder.

A catheter adapter may include a distal end, a proximal end, an inner surface extending through the distal end and the proximal end and forming a lumen, and a side port forming a side port pathway through a sidewall of the catheter adapter and in fluid communication with the lumen. The catheter assembly may include a catheter extending distally from the distal end of the catheter adapter. The catheter assembly may include a septum disposed within the lumen proximal to the side port pathway. The catheter assembly may include one or more features to facilitate flushing of the catheter assembly: a diameter of the side port may increase in a distal direction; a portion of the inner surface proximal to the catheter and distal to the septum may include multiple grooves; the side port pathway may include a non-cylindrical portion; an insert; a rotation element; and a pivot element.

A catheter system is disclosed that includes a catheter with an elongated, flexible tube having an entry end, an exit end, and a control valve. The control valve controls the flow of fluids through the catheter tube. The exit end or control valve also includes a coupler which is utilized to allow the catheter to be moved between a stowed condition coupled to a flexible belt and an in-use condition uncoupled from the belt.