Abstract: A securing device is installable on an outer circumferential surface of a nuclear reactor core shroud and in contact with an inner circumferential surface of a pressure vessel. The securing device includes a base configured for contacting the outer circumferential surface of the nuclear reactor core shroud. The securing device also includes a radial extender including an actuator, a stationary support section fixed to the base and a movable contact section. The radial extender is configured such that the movable contact section is movable along the stationary support section by the actuator to force the movable contact section radially into the inner circumferential surface of the pressure vessel.

Abstract: A securing device is installable on an outer circumferential surface of a nuclear reactor core shroud and in contact with an inner circumferential surface of a pressure vessel. The securing device includes a base configured for contacting the outer circumferential surface of the nuclear reactor core shroud. The securing device also includes a radial extender including an actuator, a stationary support section fixed to the base and a movable contact section. The radial extender is configured such that the movable contact section is movable along the stationary support section by the actuator to force the movable contact section radially into the inner circumferential surface of the pressure vessel.

Abstract: An endoprosthesis for deployment within a body passage includes a framework and a metallic film, which can circumferentially surround the framework or be surrounded by the framework. The framework and metallic film can be attached without using a third material, e.g., without sewing. The framework can define a circumferential recess along at least a portion of its length and circumference. The recess accommodates at least a portion of the metallic film therein.

Abstract: An endoprosthesis for deployment within a body passage includes a framework and a metallic film, which can circumferentially surround the framework or be surrounded by the framework. The framework and metallic film can be attached without using a third material, e.g., without sewing. The framework can define a circumferential recess along at least a portion of its length and circumference. The recess accommodates at least a portion of the metallic film therein.

Abstract: An endoprosthesis for deployment within a body passage includes an external tubular framework disposed about a tubular member, e.g., a metallic film having a thickness of about 50 ?m or less. The tubular member may be sandwiched between the external tubular framework and an internal tubular framework located internally of the external tubular framework and the tubular member. Whether or not the internal tubular framework is included, the endoprosthesis can be self-expanding. During deployment of the endoprosthesis using a deployment device, the external tubular framework prevents substantial frictional contact between the deployment device and the tubular member.

Abstract: Implantable medical endoprosthesis delivery systems and articles are provided.

Abstract: An implantable vascular prosthesis is provided for use in a wide range of applications wherein at least first and second helical sections having alternating directions of rotation are coupled to one another. The alternating helical section includes a first and second helical portions each having a flange and having adjacent ends joined directly to one another to define an apex. Each helical portion has a widened flange portion adjacent to the apex, the widened flange portions extending into a space between the helical portions. The prosthesis is configured to conform to a vessel wall without substantially remodeling the vessel, and permits accurate deployment in a vessel without shifting or foreshortening.

Abstract: An implantable vascular prosthesis is provided for use in a wide range of applications wherein at least first and second helical sections having alternating directions of rotation are coupled to one another. The prosthesis is configured to conform to a vessel wall without substantially remodeling the vessel, and permits accurate deployment in a vessel without shifting or foreshortening.

Abstract: Implantable medical endoprosthesis delivery systems and articles are provided.

Abstract: An inventive repositionable stent may comprise a plurality of adjacent serpentine bands connected to one another by at least one permanent connector strut and by at least one disengagable connector strut. The stent may self-expand within a bodily lumen to an intermediate deployment diameter, wherein the stent is constrained from further expansion by the at least one disengagable connector strut. The stent may be repositioned within the bodily lumen while in the intermediate deployment configuration. The disengagable connector strut may be disengaged via electrolytic detachment, whereupon the stent may expand to a full deployment diameter.

Abstract: Implantable medical endoprosthesis delivery systems and articles are provided.

Abstract: A vascular graft includes a vessel structure having outer and inner wall surfaces. The vessel structure has outer and inner transverse dimensions. The vascular graft includes a fold structure which is integral with the vessel structure. The fold structure extends from the outer or inner wall surface of the vessel structure for altering the inner or outer transverse dimension thereof. A method for making the vascular graft facilitates formation of the fold structure.

Abstract: An implantable vascular prosthesis is provided for use in a wide range of applications wherein at least first and second helical sections having alternating directions of rotation are coupled to one another. The prosthesis is configured to conform to a vessel wall without substantially remodeling the vessel, and permits accurate deployment in a vessel without shifting or foreshortening.

Abstract: An implantable vascular prosthesis is provided for use in a wide range of applications wherein at least first and second helical sections having alternating directions of rotation are coupled to one another. The prosthesis is configured to conform to a vessel wall without substantially remodeling the vessel, and permits accurate deployment in a vessel without shifting or foreshortening.

Abstract: An improved shell-and-tube steam instantaneous heat exchange system of a closely coupled feedback design which overheats water in the heat exchanger portion of the system and then blends the water, as needed, with proportional amounts of cold water to achieve the correct outlet temperature for a wide range of flow rates. The system uses at least two primary heat exchangers to provide redundancy in the case of failure of a major component of the system. Steam flow through the heat exchangers is controlled by the use of steam traps, rather than using a thermostatically controlled valve to vary the supply of steam. To obtain precise temperature control during varying water volume use, water is directed from the blended outlet of a first water tempering valve into the hot inlet port of a second water tempering valve.

Abstract: Implantable medical endoprosthesis delivery systems and articles are provided.

Abstract: An improved shell-and-tube steam instantaneous heat exchange system of a closely coupled feedback design which overheats water in the heat exchanger portion of the system and then blends the water, as needed, with proportional amounts of cold water to achieve the correct outlet temperature for a wide range of flow rates. The system uses at least two primary heat exchangers to provide redundancy in the case of failure of a major component of the system. Steam flow through the heat exchangers is controlled by the use of steam traps, rather than using a thermostatically controlled valve to vary the supply of steam. To obtain precise temperature control during varying water volume use, water is directed from the blended outlet of a first water tempering valve into the hot inlet port of a second water tempering valve.

Abstract: A vascular graft includes a vessel structure having outer and inner wall surfaces. The vessel structure has outer and inner transverse dimensions. The vascular graft includes a fold structure which is integral with the vessel structure. The fold structure extends from the outer or inner wall surface of the vessel structure for altering the inner or outer transverse dimension thereof. A method for making the vascular graft facilitates formation of the fold structure.

Abstract: An endoprosthesis for deployment within a body passage includes an external tubular framework disposed about a tubular member, e.g., a metallic film having a thickness of about 50 ?m or less. The tubular member may be sandwiched between the external tubular framework and an internal tubular framework located internally of the external tubular framework and the tubular member. Whether or not the internal tubular framework is included, the endoprosthesis can be self-expanding. During deployment of the endoprosthesis using a deployment device, the external tubular framework prevents substantial frictional contact between the deployment device and the tubular member.

Abstract: A medical device comprises a catheter having a balloon positioned thereon, a stent and a sheath. The sheath is disposed about the stent when the stent is in a reduced diameter configuration. When the stent is in the reduced diameter configuration it is disposed about a portion of the catheter distally adjacent to the balloon. The catheter is moveable relative to the sheath.