Abstract: A medical device and method of providing same, comprises a first stent body and a second stent body wherein the medical device is formed when the at least one first marker portion and the at least one second marker portion of the stent bodies are positioned in a predetermined alignment wherein the first stent body and the second stent body are aligned along substantially the same longitudinal axis and at least a portion of the first end region and at least a portion of the second end region of the respective stent bodies are overlappingly arranged to provide the medical device with a longitudinal length that is less than the sum of the first stent body length and the second stent body length.

Abstract: A medical device and method of providing same, comprises a first stent body and a second stent body wherein the medical device is formed when the at least one first marker portion and the at least one second marker portion of the stent bodies are positioned in a predetermined alignment wherein the first stent body and the second stent body are aligned along substantially the same longitudinal axis and at least a portion of the first end region and at least a portion of the second end region of the respective stent bodies are overlappingly arranged to provide the medical device with a longitudinal length that is less than the sum of the first stent body length and the second stent body length.

Abstract: A method and device for implanting an endoprosthesis within the lumen of a body passageway. A tubular, elongated endoprosthesis having a small outer diameter for intraluminal delivery of the selected body passageway, is capable of being progressively permanently deformed to an expanded diameter by application of outwardly acting force. The endoprosthesis is provided on a catheter having an inflatable, radially expandable balloon, the axial dimension of which is shorter than the axial dimension of the endoprosthesis. The elongated prothesis is inserted in unexpanded state into a desired location within the body passageway and with the catheter positioned so that its expandable portion registers inside a first portion of the endoprosthesis, the inflatable portion of the catheter is inflated to cause deformation of the first portion of the endoprosthesis to an expanded diameter.

Abstract: An inflatable medical device and method for the placement of a stent in a body passageway by means of a two stage expansion of the stent and for the delivery of medications to precise location in the passageway. The device includes a catheter shaft (14) having a plurality of lumens (13, 22, 28) disposed therein. The catheter shaft has a distal end adapted to be disposed within a vascular passageway. An inflatable balloon is defined by a generally cylindrical wall and is adapted to receive inflation fluids. The balloon is disposed on the distal end of the shaft. An array of circumferentially arranged inflation conduits (40) is disposed in the wall. The conduits (40) are spaced from each other within the wall of the balloon whereby to form a annular array. An array of medication delivering conduits (25) can be disposed within the wall of the balloon. These conduits are adapted to deliver medications to predetermined locations within the body passageway being treated.

Abstract: An inflatable medical device and method for the placement of a stent in a body passageway by means of a two stage expansion of the stent and for the delivery of medications to precise location in the passageway. The device includes a catheter shaft (14) having a plurality of lumens (13, 22, 28) disposed therein. The catheter shaft has a distal end adapted to be disposed within a vascular passageway. An inflatable balloon is defined by a generally cylindrical wall and is adapted to receive inflation fluids. The balloon is disposed on the distal end of the shaft. An array of circumferentially arranged inflation conduits (40) is disposed in the wall. The conduits (40) are spaced from each other within the wall of the balloon whereby to form a annular array. An array of medication delivering conduits (25) can be disposed within the wall of the balloon. These conduits are adapted to deliver medications to predetermined locations within the body passageway being treated.

Abstract: A catheter for insertion into a bodily conduit, especially an artery. The catheter comprises a shaft (26) having at least one lumen (24) for delivery of a fluid inflation media and a double balloon (12) including an array (20) of a plurality of inflatable secondary chambers (22) radially disposed in a cylindrical array around an inflatable primary chamber (16). Each of the secondary chambers (22) shares a common wall (38) with adjacent secondary chambers (22) and a common wall (14) with the primary chamber (16). The secondary chambers (22) are inflated by an array of channels (32) which are separated from each other by webs (40). One or more of the secondary chambers (22) may be in communication with a pressure transducer for measurement of the resistance of, e.g., a stenosis to dilation by the balloon (12). Alternately, a triple balloon (60) has inner secondary chambers (22a) and outer secondary chambers (22b).

Abstract: A diseased site, such as vascular dilatation site, is treated by first locally delivering to the site an agent that is effective to localize a desired drug and then systematically administering the drug.

Abstract: A method and device for implanting an endoprosthesis within the lumen of a body passageway. A tubular, elongated endoprosthesis having a small outer diameter for intraluminal delivery of the selected body passageway, is capable of being progressively permanently deformed to an expanded diameter by application of outwardly acting force. The endoprosthesis is provided on a catheter having an inflatable, radially expandable balloon, the axial dimension of which is shorter than the axial dimension of the endoprosthesis. The elongated prothesis is inserted in unexpanded state into a desired location within the body passageway and with the catheter positioned so that its expandable portion registers inside a first portion of the endoprosthesis, the inflatable portion of the catheter is inflated to cause deformation of the first portion of the endoprosthesis to an expanded diameter.

Abstract: An ultrasound imaging device and method employing it featuring a stationary, elongated flexible tubular body, a rotatable drive shaft extending through the body, and a nose member located distally of the tubular body, the nose member mounted on the distal end of the drive shaft to rotate therewith, the nose member being of rounded atraumatic form, sized at its proximal end to substantially match the diameter of the body and an acoustic imaging transducer incorporated in the nose member for producing acoustic images of adjacent tissue as the drive shaft turns, there being an axial passage within the body for fluid flow from a proximal entry port to at least one fluid delivery port located distally of the entry port.

Abstract: An ultrasound imaging device has a stationary, elongated flexible tubular body, a rotatable drive shaft extending through the body, and a nose member located distally of the tubular body. The nose member is mounted on the distal end of the drive shaft to rotate therewith, and an acoustic imaging instrument is incorporated in the nose member for producing acoustic images of adjacent tissue as the drive shaft turns. The nose member is covered with a bio-compatible, acoustically transparent, lubricous coating of hydrophilic material sufficient to shield and space the nose member from the adjacent tissue. The lubricous coating of hydrophilic material covers an area of the surface of the ultrasound imaging device through which the acoustic imaging instrument causes acoustic signals to pass. The coating has sufficient thickness to avoid puncturing of a wall of a blood vessel by the nose member while the nose member rotates within the blood vessel sufficiently close to the wall for puncturing otherwise to occur.