Embodiments herein relate to catheters including multiple braid layers. In an embodiment, a catheter is included having a catheter body, the catheter body can include a proximal end portion; a distal end portion; an inner liner; and a braided structure, the braided structure can include an inner braid layer, the inner braid layer can include a first set of inner wires; and a second set of inner wires; an outer braid layer, the outer braid layer can include a first set of outer wires; and a second set of outer wires; wherein the braided structure is disposed over the inner liner; wherein the first set of inner wires are larger than the second set of inner wires; and wherein the first set of outer wires are larger than the second set of outer wires. Other embodiments are also included herein.

A flexing structure for an insertion tube of a medical device including tubular vertebrae with a proximal tubular vertebra and a distal tubular vertebra and at least one actuating cable surrounded by a sheath over at least part of its length, the flexing structure including a tube cut with energy-beam cutting lines to create tubular vertebrae that nest in one another, the proximal tubular vertebra including, for each actuating cable, a radial and axial blocking system for the sheath, comprising an elongate cutout created in such a way as to delimit two stop edges that limit the radial engagement of the sheath in the cutout, this cutout opening at its distal part into a slot delimited by at least two cutout lines between which there is attached a pressing tab designed to press the sheath radially against the two stop edges of the cutout, this slot being bordered by a rim for axially stopping the sheath.

A system that includes a cannula and a flexible hypotube attached to the cannula configured to slidably receive an optical fiber. The system may be configured to have a ratio R1 of a diameter of the outer surface of the hypotube to a diameter of the inner surface of the cannula is 1:5>R1>1:25, and/or where the flexible hypotube comprises a tubular portion containing at least one cut extending from the outer surface at least partially through the sidewall of the flexible hypotube, each cut having a maximum width of between 0.01 and 0.1 mm.

The disclosure relates to cannulae, delivery systems, methods of making cannulae, and methods of making delivery systems. A delivery system comprises an elongate outer tubular member defining an outer tubular member lumen, a cannula having a circumferential wall extending between a proximal end and a distal end and defining an interior lumen, and an intraluminal medical device disposed within the outer tubular member lumen distal to the cannula and not about the cannula. A pattern of openings arranged in an interrupted spiral extends circumferentially along the cannula.

A pre-curved catheter tube of a catheter assembly or other elongate medical device and methods for forming such a device using a heating procedure is disclosed. Pre-curving of the catheter tube is desirable to impart to the catheter assembly a desired positional configuration when the catheter assembly is inserted into a patient. The heating procedure may include heat sterilization procedures commonly used to sterilize medical devices prior to use. One method for curving a catheter tube of a catheter assembly includes constraining the catheter tube into a curved configuration using the tube constraint, heating the catheter tube in the curved configuration for a predetermined time at a predetermined temperature, and releasing the catheter tube from the tube constraint after the heating is complete.

An enhanced flexibility catheter shaft having an elongate flexible body with a proximal end, a distal end, and at least one lumen extending therethrough. A distal, flexible section on the body has a ribbed or corrugated tubular membrane having at least a first reinforcement structure, such as a first helical support, on a radially exterior or interior surface of the membrane and optionally a second reinforcement structure, such as a second helical support, on the other of the radially interior or exterior surface of the membrane

Catheter and methods for designing, making, and using catheters are disclosed. An example catheter is a balloon catheter. The balloon catheter may include a proximal shaft. The proximal shaft may be a bare metal hypotube having a skew value of −1.0 to −2.5. A midshaft may be attached to the proximal shaft. A distal shaft may be attached to the midshaft. A balloon may be coupled to the distal shaft. An inflation lumen may be defined that extends from the proximal shaft, through the midshaft, and into the distal shaft. The inflation lumen may be in fluid communication with the balloon.

A device for repair of a heart valve leaflet includes an elongated catheter assembly having a proximal end and a distal end, and a tip at the distal end of the catheter assembly. A capture mechanism having a first free end and a second free end is rotatably coupled to a distal end of the tip. A plication mechanism has an open configuration and a closed configuration, and extends between the first free end and the second free end of the capture mechanism when in the open configuration. The device may also include a clip housing at a proximal end of the tip configured to hold a clip therein.

An implantable medical device (IMD) can include implantable pulse generator (IPG) devices, implantable cardioverter-defibrillators (ICD), cardiac resynchronization therapy defibrillator devices, neurostimulators or combinations thereof. In one example, the IMD can include a body assembly, which can provide at least one electrical signal corresponding to a therapy. The IMD can also include a cardiac lead assembly, which can have a proximal portion and a distal portion. The proximal portion of the cardiac lead assembly can be in communication with the body assembly to receive the therapy and the distal portion can be adapted to be coupled to an anatomical structure to transmit the at least one electrical signal to the anatomical structure. The proximal portion of the cardiac lead assembly can have a first stiffness and the distal portion can have a second stiffness. The first stiffness can be greater than the second stiffness.

Provided herein are dual-lumen catheters, systems, and methods thereof. In some embodiments, for example, a catheter assembly configured for modifying intravascular lesions is provided including a core wire, a dual-lumen extrusion including the core wire, and a manifold disposed around a portion of the dual-lumen extrusion. The core wire includes a proximal end configured to vibrationally couple to an ultrasound transducer. The dual-lumen extrusion includes a first lumen and a second lumen. The core wire is disposed within the first lumen, and the second lumen is configured to accommodate a guidewire. The manifold is disposed around at least a skived proximal-end portion of the dual-lumen extrusion, wherein the skived portion includes the second lumen without the first lumen. In some embodiments, the catheter assembly further includes the ultrasound transducer. In some embodiments, a system console includes the ultrasound transducer.