An endoprosthesis constraining sleeve includes a single sheet of material forming at least two folds, and a common bond line constraining the single sheet of material to maintain the at least two folds and to form at least two discrete lumens. A first lumen of the at least two lumens is configured to receive a constrained endoprosthesis therein. A second lumen of the at least two lumens is configured to receive a control feature therethrough.

A system for delivery of a medical device includes a delivery member and a medical device, which is mounted to the delivery member and releasably retained in a delivery configuration for endoluminal delivery of the medical device toward a treatment site in a human vessel. The delivery member includes an elongated first portion configured to extend outside of the body from a first percutaneous access site and an elongated second portion configured to extend outside the body from a second percutaneous access site to allow positioning of the medical device at the treatment site by manipulation of the first portion and second portion from outside of the body.

A system for delivery of a medical device includes a delivery member and a medical device, which is mounted to the delivery member and releasably retained in a delivery configuration for endoluminal delivery of the medical device toward a treatment site in a human vessel. The delivery member includes an elongated first portion configured to extend outside of the body from a first percutaneous access site and an elongated second portion configured to extend outside the body from a second percutaneous access site to allow positioning of the medical device at the treatment site by manipulation of the first portion and second portion from outside of the body.

A medical device is disclosed for delivering a medical member which is intended to indwell in a treatment site of a urethra includes a flexible main body that extends in an axial direction, a balloon that includes an effectively dilatable portion on which the medical member is mounted, that has a dilating space into which a pressurizing medium flows between an outer surface of the main body and the balloon, and that is capable of dilating deformation and deflating deformation, an elongated guide member that is arranged across the treatment site and the outside of a living body via the urethra, and an attachment portion to which at least a portion of the guide member is detachably attached at a position between both end portions in the axial direction of the main body.

An endoprosthesis constraining sleeve includes a single sheet of material forming at least two folds, and a common bond line constraining the single sheet of material to maintain the at least two folds and to form at least two discrete lumens. A first lumen of the at least two lumens is configured to receive a constrained endoprosthesis therein. A second lumen of the at least two lumens is configured to receive a control feature therethrough.

An endoprosthesis constraining sleeve includes a single sheet of material forming at least two folds, and a common bond line constraining the single sheet of material to maintain the at least two folds and to form at least two discrete lumens. A first lumen of the at least two lumens is configured to receive a constrained endoprosthesis therein. A second lumen of the at least two lumens is configured to receive a control feature therethrough.

A stent comprises a first longitudinally extended cylindrical-shaped member. The first member comprises a plurality of first longitudinal struts and an array of first radial struts extending between the first longitudinal struts. The stent further comprises an overlapping region to form a dense mesh.

A stent comprises a first longitudinally extended cylindrical-shaped member. The first member comprises a plurality of first longitudinal struts and an array of first radial struts extending between the first longitudinal struts. The stent further comprises an overlapping region to form a dense mesh.

A stent with a common connection interface, and a method and platform used to create a stent with a common connection interface is described. A common connection interface used to connect a stent to a pusher is described.

A stent with a common connection interface, and a method and platform used to create a stent with a common connection interface is described. A common connection interface used to connect a stent to a pusher is described.