A delivery catheter for implanting a self-expanding implant such as a cardiovascular implant. An outer catheter shaft is formed as an implant capsule for encasing the implant during delivery. A flexible distal support element having a substantially truncated cone-shaped portion, which tapers in the proximal direction, is attached, directly proximally of the implant, in a fixed position to a first, inner catheter shaft, and/or a flexible proximal support element having a substantially truncated cone-shaped portion, which tapers in the proximal direction, is inserted at the proximal end of the implant capsule into the second, outer catheter shaft in a fixed position.

Devices used to provide access the vasculature are disclosed. The devices may be configured to provide access to a blood vessel, such as an artery. The devices may include a catheter assembly disposed over a needle assembly. The devices may also include a barrel assembly coupled to the needle assembly. A guidewire may be displaceable by barrel assembly within a needle. The needle may include a proximal and distal port.

Aspects of the present disclosure include catheter devices in which a bushing is disposed in an interior cavity of a catheter hub. The bushing has a flexible portion extending out a distal end of the catheter hub. A catheter tube is sleeved over the flexible portion. A needle hub with a needle projects through the flexible portion of the bushing and the catheter tube. The flexible portion is bendable to form at least one curve along the flexible portion. The at least one curve has a minimum bend radius when a first surface of the flexible portion is extended and a second surface opposite the first surface of the flexible portion is shortened.

A catheter that is configured to achieve high velocity injections of contrast solution that will not readily wash out in retrograde blood flow. The distal end of the catheter can include a plurality of fluid outlet openings. The fluid outlet openings are spaced circumferentially around the circumference of the catheter and the fluid outlet openings have ejection axes that are angled in a direction toward the distal end so that a velocity component of the ejected contrast solution is against or opposite the retrograde blood flow.

A spool and gear mechanism for tensioning and manipulating the steering/deflection control wires of a steerable catheter device provides for a desired level of tension that will allow operation of the device without too little or too much tension in those wires. In a wire-tensioning mechanism for a steerable catheter, the mechanism includes at least a first and second steering/deflection control wire each attached to the spool by winding around its own detent-engaged rotatable gear in the spool and extending out through a radial wall of the spool to engage into a steerable catheter body. In a multi-spool system, the wire-tensioning/winding gears of each spool preferably are accessible for adjustment via apertures of an adjacent spool.

A high torque vascular catheter system includes an inner catheter, a proximal outer catheter section, a distal outer catheter section, at least one discrete connection point connecting the inner catheter to the proximal outer catheter section, and at least one discrete connection point connecting the inner catheter to the distal outer catheter section. The distal outer catheter section is more flexible than the proximal outer catheter section. Methods of construction and use of the catheter system are also disclosed.

In a catheter system and method for controlling such a system, an elongate hollow shaft has a proximal end connected to a handle and a distal end remote from the handle. A working component is carried by the shaft and has at least one characteristic that is adjustable. An actuator is rotatably mounted on the handle for selectively adjusting at least one characteristic of the working component. A control line extends at least in part within the shaft. The control line operatively couples the actuator with the working component such that rotation of the actuator relative to the handle effects linear translation of the control line to adjust the at least one characteristic of the working component.

An anchor strain relief member provides resistance to disengagement from a hemostatic valve due to forces tending to force the catheter in a proximal direction. The anchoring strain relief member is distal to a hub, joined to the catheter outer surface, and comprises a sealing portion that has at least one ridge that has a ridge tip and a ridge height defined by a distance from the ridge tip to the catheter central axis. Methods of forming a nested catheter system are described using a catheter with an anchor strain relief as the inner catheter for the nested catheter set. Systems of a hemostatic valve and a suitable catheter with an anchor strain relief member can provide for desired assemblies of components.

Use of embolic material that is biodegradable provides for embolizing a hypervascular vessel formed in response to chronic inflammation in a musculoskeletal vasculature or a vessel related to production of ghrelin. The embolic material is biodegradable within a predetermined period of time. Medical systems are configured for delivery of embolic material for embolizing the hypervascular vessel or the vessel related to production of ghrelin.

Embodiments disclosed herein relate to an aspiration catheter comprising a catheter body that can have a first end and a second end and an aspiration lumen extending through the catheter body. The aspiration lumen can have an aspiration opening located in a distal portion of the aspiration catheter. The catheter can have an assistive jet element extending through a wall of the aspiration lumen. The assistive jet element can have an assistive jet channel. The assistive jet element can be adaptable to draw blood through the assistive jet element from a location outside of the catheter body adjacent to the assistive jet element and into the aspiration lumen when suction is applied to the aspiration lumen and can be configured to break apart a thrombus or obstruction in the aspiration lumen.