A stent according to the invention includes: a strut extending in a predetermined direction; a first protrusion provided on the strut, the first protrusion being substantially L-shaped and extending in a direction away from the strut and in a direction toward a distal side in the predetermined direction; a second protrusion that is provided on the strut and located distal to the first protrusion, the second protrusion being substantially L-shaped, extending in a direction away from the strut and in a direction toward a proximal side in the predetermined direction, and having a tip spaced apart from a tip of the first protrusion; and an opaque member being substantially tubular and highly opaque to radiation, the opaque member having two end portions in which the first and second protrusions are inserted, respectively.

A system for deploying a shape memory catheterization device within a patient, includes a catheter for endovascular insertion of the shape memory catheterization device. A heat source heats the shape memory catheterization device above the transition temperature. A transformation data generator includes a circuit driver for driving a circuit that includes at least one capacitive element of the shape memory catheterization device and a detection circuit for generating transformation data based on a capacitance of the at least one capacitive element, wherein the transformation data indicates a shape transformation of the shape memory catheterization device from a catheterization shape to a transformed shape.

A delivery system for delivering a prosthesis includes a spindle for securing a stent to a shaft. The spindle includes at least one pocket for receiving a paddle of the stent. The delivery system also includes at least one sensor positioned within the at least one pocket and configured to detect a presence of the paddle relative to the at least one pocket.

Example aspects of a deployment probe for deploying a stent, a pipe repair assembly, and a method for repairing a pipeline are disclosed. The deployment probe for deploying a stent can comprise a probe body defining an inner surface, an outer surface, and a slot extending from the inner surface to the outer surface, the inner surface defining a probe void, the probe void defining a probe axis, the slot extending in an axial direction relative to the probe axis; and a release mechanism comprising a retainer body received within the probe void and a stent retainer coupled to the retainer body, the stent retainer substantially aligned with the slot and configured to engage a stent.

A delivery catheter for a stent valve, the delivery catheter having a distal portion insertable into an anatomy, the distal portion comprising an accommodation region for accommodating a stent-valve for delivery into the anatomy, the delivery catheter further comprising at least one sheath that is translatable between a closed position for at least partly closing the accommodation region and an open position for at least partly opening the accommodation region.

Controlled deployable medical devices that are retained inside a body passage and in one particular application to vascular devices used in repairing arterial dilations, e.g., aneurysms. Such devices can be adjusted during deployment, thereby allowing at least one of a longitudinal or radial re-positioning, resulting in precise alignment of the device to an implant target site.

A device and a method for treatment of a urethra that is constricted due to benign prostatic hyperplasia (BPH) are provided, including a delivery tool (101) advanced to a location in an area of the urethra that is to be treated. The delivery tool (101) includes an expandable element (400) that expands within the urethra such as to enlarge the urethra, a tissue cutter (412) that forms a cut in the urethra, subsequently to the expandable element expanding to dilate the urethra, and an implant (410) that maintain the urethra in a dilated state. The implant (410) includes a shape-memory material and is shaped to define two end sections and a middle section (1202) disposed between the two end sections. The shape memory-material is shape set such that in an unconstrained configuration of the implant (410), the middle section (1202) is substantially straight. Other embodiments are also described.

The present embodiments provide systems and methods for improved retention of stents on a delivery system. In one embodiment, a delivery system comprises a catheter and a balloon. A proximal end of the balloon is secured to an exterior surface of the catheter at a first location, and a distal end of the balloon is secured to the exterior surface of the catheter at a second location. A plurality of bands are disposed in a circumferential space situated between the exterior surface of the catheter and an interior surface of the balloon. The plurality of bands may comprise at least four bands that are discretely spaced-apart in an axial direction from one another along a length of the catheter. At least one stent is secured to the exterior surface of the balloon in a compressed delivery state.

A method of deploying an implantable stented device in an anatomical location of a patient, including the steps of providing a delivery system with first and second stent engagement structures at its distal end, attaching a first structural element of the stented device to the first stent engagement structure and attaching a second structural element of the stented device to the second silent engagement structure, advancing the stented device to an implantation site, and sequentially disengaging the first structural element of the stented device from the first stent engagement structure of the delivery system and then disengaging the second structural element of the stented device from the second stent engagement structure.

A delivery system is provided for self-expanding medical devices, such as stents. The delivery system has a restraining sheath that maintains the stent in a compressed state prior to deployment. The restraining sheath terminates distally from the deployment handle, and a wire connects the restraining sheath to the deployment handle. The restraining sheath is withdrawn from the stent to deploy the stent by pulling the wires proximally at the deployment handle.