The present invention provides a stent delivery assembly including: a catheter including a shaft having a proximal end and a distal end, and a balloon provided closer to the proximal end than the distal end on the shaft; and a stent having a tubular shape, and coupled to the balloon to surround an outer circumferential surface of the balloon, wherein the balloon includes a main body having a first end and a second end, the stent is located to be biased towards the first end, such that the main body includes a preferential inflation region exposed to the outside between the second end and the stent, the main body is formed to extend with a diameter that is constant from the first end to the second end, and while the balloon is inflated, a portion of the stent close to the preferential inflation region is inflated in a tapered shape by a force caused when the preferential inflation region is preferentially inflated.

The present invention provides a stent delivery assembly including: a catheter including a shaft having a proximal end and a distal end, and a balloon provided closer to the proximal end than the distal end on the shaft; and a stent having a tubular shape, and coupled to the balloon to surround an outer circumferential surface of the balloon, wherein the balloon includes a main body having a first end and a second end, the stent is located to be biased towards the first end, such that the main body includes a preferential inflation region exposed to the outside between the second end and the stent, the main body is formed to extend with a diameter that is constant from the first end to the second end, and while the balloon is inflated, a portion of the stent close to the preferential inflation region is inflated in a tapered shape by a force caused when the preferential inflation region is preferentially inflated.

An ostial stent delivery device may include a first elongate shaft including a first lumen and extending along a central longitudinal axis, wherein the first elongate shaft includes a first inflatable balloon fixedly attached proximate a distal end of the first elongate shaft; and a second elongate shaft including a second lumen, the first elongate shaft being at least partially disposed within the second lumen. The second elongate shaft includes a second inflatable balloon fixedly attached proximate a distal end of the second elongate shaft. The second inflatable balloon is disposed at least partially proximal of the first inflatable balloon. The first inflatable balloon has a substantially cylindrical shape along a majority of its length in the deployed configuration. The second inflatable balloon has a substantially biconical shape having a central axis oriented parallel to the central longitudinal axis in the deployed configuration.

An ostial stent delivery device may include a first elongate shaft including a first lumen and extending along a central longitudinal axis, wherein the first elongate shaft includes a first inflatable balloon fixedly attached proximate a distal end of the first elongate shaft; and a second elongate shaft including a second lumen, the first elongate shaft being at least partially disposed within the second lumen. The second elongate shaft includes a second inflatable balloon fixedly attached proximate a distal end of the second elongate shaft. The second inflatable balloon is disposed at least partially proximal of the first inflatable balloon. The first inflatable balloon has a substantially cylindrical shape along a majority of its length in the deployed configuration. The second inflatable balloon has a substantially biconical shape having a central axis oriented parallel to the central longitudinal axis in the deployed configuration.

A venous stent may be used to maintain or enhance patency of a blood vessel. By using multiple, separate stent elements that are balloon expandable, the multi-element stent may be stronger than a traditional self-expanding stent but may also be more flexible, due to its multiple-element configuration, than a traditional balloon-expandable stent. The stent elements are formed from a bioresorbable polymer material. The stent elements may have thick and/or wide struts and may be deployed oversized so as to overcome venous elastic recoil and anatomic compression.

A stent delivery system for treating a bifurcated vessel includes a first elongate shaft with a first expandable member. A first stent having a side hole is disposed over the first expandable member. A second elongate shaft has a second expandable member. The second elongate shaft is slidably disposed under the proximal end of the first stent and extends out of the side hole. The first stent is fully crimped over a proximal portion and a distal portion of the first expandable member and a proximal portion of the second expandable member so as to prevent axial movement of the first stent relative to the first or second elongate shafts during delivery. Portions of the first or second expandable members may be pillowed to provide a protective barrier that prevents edges of the stent from catching on other objects.

A stent delivery system for treating a bifurcated vessel includes a first elongate shaft with a first expandable member. A first stent having a side hole is disposed over the first expandable member. A second elongate shaft has a second expandable member. The second elongate shaft is slidably disposed under the proximal end of the first stent and extends out of the side hole. The first stent is fully crimped over a proximal portion and a distal portion of the first expandable member and a proximal portion of the second expandable member so as to prevent axial movement of the first stent relative to the first or second elongate shafts during delivery. Portions of the first or second expandable members may be pillowed to provide a protective barrier that prevents edges of the stent from catching on other objects.

Embodiments of the present invention provide a unique new approach to generating operating condition information used for assessing flow assurance and structural integrity. More specifically, apparatuses, systems and sensor housing assemblies configured in accordance with embodiments of the present invention utilize fiber optic sensors for enabling monitoring of operating condition information within one or more elongated tubular members within a subsea environment. To this end, such fiber optic sensors connected by lengths of optical fiber are strategically placed at a plurality of locations along a length of each elongated tubular member thereby allowing critical operating conditions such as strain, temperature and pressure of the elongated tubular member and/or a fluid therein to be monitored. A viscous media is used for mitigating attenuation associated with exposure of optical fiber exposed to forces generated by pressure within the subsea environment.

A method and an assembly for securing a crimped medical device over a deflated balloon of a balloon catheter is provided. The medical device is positioned in its expanded state over the deflated balloon of the balloon catheter, and is then crimped over the deflated balloon. First and second eyelets of first and second strings, respectively, are then threaded through first and second rings, respectively, that are provided on the medical device. Next, a locking wire is advanced through a lumen defined between the sheath and the catheter body to exit the distal end of the sheath, and then advanced through the first and second eyelets and into the distal tip of the balloon catheter. The sheath is then advanced over the crimped medical device to the distal tip to completely cover the crimped medical device.

A method and an assembly for securing a crimped medical device over a deflated balloon of a balloon catheter is provided. The medical device is positioned in its expanded state over the deflated balloon of the balloon catheter, and is then crimped over the deflated balloon. First and second eyelets of first and second strings, respectively, are then threaded through first and second rings, respectively, that are provided on the medical device. Next, a locking wire is advanced through a lumen defined between the sheath and the catheter body to exit the distal end of the sheath, and then advanced through the first and second eyelets and into the distal tip of the balloon catheter. The sheath is then advanced over the crimped medical device to the distal tip to completely cover the crimped medical device.