A device comprises a tubular member with a longitudinal axis having a proximal end and a distal end, at least one partial cut located at, along or near the distal end of the tubular member, the at least one partial cut comprising an orientation that is angled relative to both the longitudinal axis and an axis transverse to the longitudinal axis, a pusher member positioned within an interior of the tubular member and configured to selectively advance the distal end of the tubular member longitudinally, wherein the distal end of the tubular member is configured to at least partially rotate when the pusher member is advanced relative to the tubular member so at to facilitate placement of the distal end in a particular branch of a subject's intraluminal network, wherein the distal end of the tubular member is configured to longitudinally elongate along or near an area of the at least one partial cut.

A catheter system may include a catheter assembly and a needle assembly. The catheter assembly may include a catheter hub and a catheter extending distally from the distal end of the catheter hub. The catheter assembly may include a cover coupled to a proximal portion of the catheter hub. The cover may be configured to reduce contact with the catheter assembly during initial insertion of the catheter assembly into vasculature of a patient and/or threading the catheter, which may reduce a risk of bacterial contamination of the catheter. The needle assembly may include an introducer needle, a housing, and a needle hub disposed within the housing. The housing may include a button. A proximal end of the introducer needle may be secured within the needle hub. In response to activation of the button, the needle hub and the introducer needle may move proximally within the housing.

A catheter assembly includes an outer shaft having an outer shaft body forming an outer shaft bore that receives an inner shaft. The outer shaft has a wire transition section. The catheter assembly includes an exit path connector coupled to the outer shaft body at the wire transition section. The exit path connector has a rigid body section separate and discrete from the outer shaft body and coupled to the outer shaft body. The body section defines an exit path connector bore that receives the inner shaft. The body section has a side exit port at a side of the body section being open to the exit path connector bore. The catheter assembly includes a catheter wire passing through the side exit port from an interior to an exterior of the cable exit port.

A rigidizing device includes an elongate flexible tube, a braid layer positioned over the elongate flexible tube, an outer layer over the flexible tube and the braid layer, and an inlet between the elongate flexible tube and the outer layer and configured to attach to a source of vacuum or pressure. The braid layer has a plurality of strands braided together at a braid angle of 5-40 degrees relative to a longitudinal axis of the elongate flexible tube when the elongate flexible tube is straight. The rigidizing device is configured to have a rigid configuration when vacuum or pressure is applied through the inlet and a flexible configuration when vacuum or pressure is not applied through the inlet. The braid angle is configured to change as the rigidizing device bends when the rigidizing device is in the flexible configuration.

A catheter assembly including a multi-luminal catheter, a primary stylet, and a secondary stylet. The primary stylet and the secondary stylet are each inserted into separate lumens extending along the catheter tube. The primary stylet includes a magnetic region to enable magnetic tracking. The secondary stylet is configured to prevent buckling of the magnetic region during insertion. The secondary stylet includes a proximal section having a proximal column strength and a distal section having a distal column strength greater than the proximal column strength. During use, an insertion force exceeding an insertion force limit causes the proximal section to buckle to prevent buckling of the distal section. The primary stylet may also include electrical sensors and/or an optical fiber configured for shape sensing.

Reinforced catheter tips, catheters including rapidly insertable central catheters (“RICCs”), and methods thereof reduce the number of steps and medical devices involved in introducing catheters into patients. In an example of a catheter, a RICC can include a catheter tube, a catheter hub coupled to a proximal portion of the catheter tube, and a plurality of extension legs extending from the catheter hub. The catheter tube can include a first section in a distal portion of the catheter tube and a second section proximal of the first section. The first section of the catheter tube can distally terminate with a catheter tip reinforced with a reinforcement band therein. The plurality of extension legs that extend from the catheter hub can be equal in number to a plurality of lumens extending through the RICC. In another example, a method can include a method of making the foregoing RICC.

A fluid transfer device for use with a peripheral intravenous catheter (PIVC) including an introducer body having a proximal end and a distal end, and a flow tube at least partially housed within the introducer body, wherein the flow tube is configured to be selectively extendable from the introducer body. The fluid transfer device also includes a lever lock coupled to the distal end of the introducer body, wherein the lever lock includes a lumen configured to allow the flow tube to pass therethrough, and wherein an effective length of the lever lock relative to the distal end of the introducer body is adjustable in order to accommodate use of the fluid transfer device with indwelling catheters of the PIVC having various lengths.

Catheter assemblies may include introducer needles having a notch or similar structure that allows flashback blood to enter the annular space between a catheter tube and an introducer needle of an IV catheter. The presence of flashback blood in this annular space can provide a clinician with an early, visible indication that a needle has entered a vein. The notch, however, may create a leak path for blood to escape outside of the catheter assembly, unless contained. Disclosed herein is a notch containment that prevents the notch from providing a leak path for blood to escape outside of the catheter during or after needle withdrawal.

An access device may be provided that includes a hub configured to improve the flow of blood within a lumen, in order to prevent, e.g., thrombus formation, while also avoiding hemolysis. The hub may have a removably attachable second arm, protrusions/depressions with the lumens of the hub or system, and/or plugs or plug analogs may be used to prevent flow from entering certain regions of the lumens within the hub. These hubs may be used, e.g., as part of an access device, which may have a modular configuration.

A catheter assembly may include a catheter hub, which may include a distal end, a proximal end, and a catheter hub lumen extending through the distal end of the catheter hub and the proximal end of the catheter hub. The catheter assembly may include a catheter extending from the distal end of the catheter hub. The catheter may include a catheter tube, which may include a distal end, a proximal end, and a catheter tube lumen extending through the distal end of the catheter tube and the proximal end of the catheter tube. The catheter may also include a fluid-permeable section extending from the distal end of the catheter tube. The fluid-permeable section may include a coil or a lattice. The catheter assembly may include an introducer needle extending through the catheter tube and the fluid-permeable section.