Abstract: A self expanding stent (10) formed from a resilient wire. The resilient wire comprises a zig zag form including an odd number of struts (12) such as seven struts and a bend (14) between each strut. There is first loop (18) of the resilient wire at the terminal end of a first strut and a second loop (18) of the resilient wire at the terminal end of a last strut. The stent as formed is substantially planar but in use is formed into a substantially cylindrical form (20) by being stitched onto a tubular body of a biocompatible graft material with at least the first strut and the last strut overlapping.

Abstract: A highly flexible delivery device (2) for a stent graft (6) particularly for deployment into the thoracic arch of a patient. The delivery device has a distal handle (7), a pusher catheter (4) extending proximally from the handle to a proximal nose cone dilator (11), a guide wire catheter (3) extending from the proximal nose cone dilator to the pusher catheter. To give flexibility the guide wire catheter comprises a Nitinol™ tube, the nose cone dilator has a high flexibility and the pusher catheter has a graded flexibility being more flexible at its proximal end than at its distal end. The graded flexibility can be provided by joined segments (4a, 4b and 4c) of different flexibility or by a inner metal tube (72) to give rigidity over some of the length. Alternatively the graded flexibility can be provided by tapering the wall thickness (80, 80a) of the pusher catheter.

Abstract: A fastening for fixing an exposed stent (2) to a graft material (1). At least two spaced apart fastenings (7, 8) are used, each fastening has at least one turn and preferably two turns of an elongate flexible fiber through the graft material and around a portion of the stent. Each fastening has a knot (9) which is at least two thumb knots and preferably four thumb knots.

Abstract: A method of sizing of a stent graft (20) including placement of fenestrations (30, 32) to ensure access to side branch vessels (13, 15) through the fenestrations when the stent graft is introduced into a body vessel and an assembly method for a stent graft including temporary diameter reduction arrangements to enable partial release of a stent graft to assist with positioning of fenestrations with respect to side branch vessels. The method includes spacing the fenestrations to be the same circumferential distance as the side branch vessels irrespective of the diameter of the stent graft.

Abstract: A thoracic stent graft (20) has a tubular bio-compatible graft material body (22) with a lumen therethrough with a proximal end (26) and a distal end (27). There is a sealing stent (28) at the proximal end of the tubular body with an anchoring device which may be a barb (30) affixed to the sealing stent. A distal attachment stent (34) with barbs (36) can be affixed to and extend from the distal end (27) of the graft material body. Intermediate stents (24) are provided along the length of the body. The thoracic stent graft can be in one or two portions.

Abstract: A stent graft introducer has a pusher, a nose cone, a region between the pusher and the nose cone for a stent graft, a sleeve extending over the pusher and proximally to the nose cone to cover the stent graft when retained in the region. An indwelling auxiliary catheter with a pre-curved proximal end is fitted into the introducer. The nose cone has an elongate groove and the auxiliary catheter has its proximal end in the elongate groove. In a partially retracted position of the sleeve the curved proximal end of the indwelling auxiliary catheter is exposed and uncovered by the sleeve and in an advanced position of the sleeve the curved proximal end of the indwelling auxiliary catheter is straightened, extends along the length of the groove in the nose cone and is covered by the sleeve.

Abstract: A system for designing and ordering a stent graft is described. The system includes a user interface for designing and ordering the stent graft, and a centralised data processor remote from and in communication with the user interface for processing and storing entered information. The user interface further includes a selection portion for selecting a stent graft design and a design portion for entering a plurality of design parameters related to the stent graft design. A verification portion is also provided to verify details of a completed stent graft design with an ordering portion to order the completed stent graft design. In one embodiment the verification portion includes the capability to display a 3-dimensional view of the completed stent graft design.

Abstract: A stent graft delivery system in which a stent graft (6) is retained on a delivery device (2) such that a longitudinal portion of the stent graft is releasably retained on the delivery device to bend therewith. The delivery device (2) has a guide wire catheter (3) and the stent graft is retained onto the guide wire catheter by a release wire (24) which can be withdrawn. The release wire is wound around the guide wire catheter and through the stent graft or suture loops engage around the guide wire catheter and release wire.

Abstract: A bung for an aspiration assembly sample collection tube, the bung (1) has a top surface (3), a tapered side surface (7) for fitting into the sample tube and a lower surface (5). First and second apertures (9, 11) extend through the bung from the top surface to the bottom surface, the first aperture (9) being for an inlet tubing and the second aperture (11) being for an aspiration tubing, the first aperture has a recess (13) in the lower surface of the bung. This recess is adapted to sealingly receive a supply nozzle of a flushing fluid supply device such as a syringe so that in use flushing fluid may be directed through the inlet tubing.

Abstract: A method of assembling of a stent graft (20) including temporarily diameter reduction arrangements to enable partial release of a stent graft to assist with positioning before complete release. The diameter reduction arrangement includes a release wire (72) and flexible threads (74, 80) extending to struts (76) of a self expanding stent (70) either side of the release wire and being pulled tight. Removal of the release wire enables full expansion of the self expanding stent.

Abstract: Disclosed is a stent graft prosthesis comprising a graft portion that includes a main body portion and an cuff portion, the cuff portion generally located at or near the proximal end of the main body portion and extending circumferentially therealong. Stents comprising the graft supporting structure are also attached to graft portion about the proximal end. In one embodiment, the cuff portion comprises material that is folded over the outside surface of the main body portion with an anchoring stent being attached over the cuff and main body portions, extending proximally therefrom. In another series of embodiments, the cuff portion comprises an external sealing zone that extends around the outer main body portion to help prevent leakage of fluids. In one example, the material of the second edge of the cuff portion is frayed to better engage the vessel walls and promote thrombus and/or tissue growth.

Abstract: A side branch stent graft (1) suitable for the iliac arteries has a main tubular body (3) of a biocompatible graft material and a tubular side branch (5). The tubular side branch is affixed into the main tubular body so that a side branch lumen is in fluid communication with a main lumen. There is at least one external zig-zag stent (13) on the main tubular body proximal of the tubular side branch, one central external stent (14) which also encompasses the side arm, at least one external zig-zag stent (16) on the main tubular body distal of the tubular side branch and one internal zig-zag stent (15) at the distal end of the main tubular body. A reinforcing ring (9) is around the proximal end of the main tubular body and stitched thereto.

Abstract: A laparoscopic vascular conduit arrangement has an elongate graft tube (1, 10) which is placed through a body cavity into a body vessel using a laparoscopic port sheath (70) with a distal valve (73) and a second sheath (80) with distal valve (86, 87). The graft tube (1, 10) extends through the laparoscopic port sheath so that the distal end (108) of the graft tube extends out of its valve and the proximal end of the graft tube extends out of the proximal end of the laparoscopic port sheath. The second sheath (80) is deployed into the distal end (108) of the graft tube (1, 10) such that the first valve (73) seals around the graft tube and the second sheath (84). The proximal end of the graft tube can be deployed into the vessel of the body to allow access into the vessel through the graft tube via the second valve. The conduit can be removed after use or used to provide vascular bypass.

Abstract: A graft (1) which is in the form of an inflatable member adapted to be formed into a predetermined and/or selected shape when deployed in situ by filling with a filler material (6) which can be made rigid in situ and deployed on a balloon catheter (12). The deployment balloon (13) is formed from a non-compliant material.

Abstract: A stent assembly (42) adapted for endoluminal placement by endovascular deployment for the treatment of a false lumen (10) associated with a vascular dissection. The stent assembly has a number of self expanding stents (35) connected together to define an elongate substantially cylindrical lumen wall engaging surface. The stents are adapted to provided pressure on the wall of the lumen adjacent to and extending away from a rupture. A deployment device (40) for the stent assembly includes a sheath (48) and a retention and release arrangement (50) to retain the proximal end (37) of the stent graft to the deployment device. Release of the stent assembly is by withdrawal of the sheath before release of its proximal end by the use of a trigger wire (54) of the retention and release arrangement.

Abstract: A stent graft (1) has a tubular body (3) defining a main lumen and a side tube (5) defining a side tube lumen and in fluid communication with the main lumen and defining a junction (13) between the tubular body and the side tube. The junction includes an acute angle of attachment (?). A first zig-zag stent (15) is wrapped around the tubular body such that a V portion of the first zig-zag stent is engaged about the acute angle of the junction and a second zig-zag stent (23) is wrapped around the side tube, such that a V portion of the second zig-zag stent is engaged about the acute angle of the junction, whereby the main lumen and the side tube are each kept open, independently, allowing fluid to flow freely therethrough.

Abstract: A connection socket (12) for an end of a stent graft or a side arm (10) of a stent graft. The connection socket has a first resilient ring (14) around the arm at its end, a second resilient ring (16) spaced apart along the arm from the first ring and optionally a zig zag resilient stent (20) between the first and second rings. Each of the rings is of slightly lesser diameter than the side arm. The zig-zag resilient stent can be a compression stent.

Abstract: A joining arrangement between a main tube (3) and a side arm (5) in a side arm stent graft (1). The side arm (5) is stitched into an aperture (11) in the main tube and is in fluid communication with it. The aperture is triangular, elliptical or rectangular and the side arm is cut off at an angle to leave an end portion having a circumferential length equal to the circumference of the aperture. The side arm can also include a connection socket (76) comprising a first resilient ring (79) around the arm at its end, a second resilient ring (80) spaced apart along the arm from the first ring and a zig zag resilient stent (82) between the first and second rings. The zig-zag resilient stent can be a compression stent. Both the main tube and the side arm are formed from seamless tubular biocompatible graft material.

Abstract: A large diameter, flexible, kink-resistant and rotatable introducer sheath (10) for percutaneous delivery of a contained and implantable medical device in the vasculature of a patient. The introducer sheath includes a reinforcement such as a flat wire coil (23) fitted about an inner, lubricous material such as polytetrafluoroethylene tube (22). A wire braid (25) is placed around the coil to give good transfer of rotational forces. An outer tube (27) of a heat formable polyamide material is heat formed and compressed through the spaces between the wires of the braid and turns of the wire coil to mechanically connect the outer tube to the roughened outer surface of the inner tube. The durometer of the outer tube can be varied to effect the flexibility of the sheath. A radiopaque marker (42) is positioned at the distal end of the coil and around the inner tube for radiographic visualization.

Abstract: A stent graft introducer for intraluminal deployment of a stent graft (26), the introducer comprising a stent graft release mechanism (6) to allow partial release of the stent graft (26) when carried on the introducer, whereby control of the stent graft can be maintained while allowing access into the lumen of the stent graft from at least one end of the stent graft. The partial release can comprise partial release of one end of the stent graft.