Abstract: Various aspects of the present invention provide compositions and implantable devices including a water-insoluble therapeutic agent solubilized in a matrix of a gallate-containing compound. Other aspects provide methods of manufacturing and using such compositions and devices.

Abstract: A scope system may comprise an elongate tube having a lumen extending therethrough. The elongate tube may have a distal portion. The scope system may further comprise at least one accessory channel extending at least partially through the lumen. The accessory channel may comprise a tubular structure having an accessory lumen extending therethrough. The accessory channel may be moveable relative to the distal portion of the elongate tube and may be configured to direct fluid to an irrigation opening located at a distal end of the accessory channel.

Abstract: Valve devices, methods of making valve devices, and methods of treating various venous-related conditions, disorders and/or diseases are described. In one embodiment, a valve device includes an expandable support frame and a bioprosthetic valve attached to the support frame. The bioprosthetic valve comprises a leaflet and a contiguous wall portion harvested from a multi-leaflet xenogeneic valve. The contiguous wall portion includes the attachment region where the leaflets attaches to the vessel wall and, in some embodiments, includes the natural margins of attachment between the leaflet and vessel wall.

Abstract: An implantable endoluminal prosthesis for replacing a damaged aortic valve is provided. In one embodiment, the prosthesis includes a balloon-expandable stent, a tubular conduit that extends into the ascending aorta, and a self-expanding stent. The tubular conduit extends across the balloon-expandable stent. The tubular conduit includes an artificial valve. The self-expanding stent extends across the tubular conduit into the ascending aorta. The balloon-expandable stent, the tubular conduit, and the self-expanding stent are coupled to provide unidirectional flow of fluid into the aorta and further into the coronary arteries. Also provided is a method for implanting the endoluminal prosthesis.

Abstract: A handle assembly for a prosthesis delivery device is disclosed. The handle assembly comprises a stationary main handle having a proximal end and a distal end and an outer surface extending therebetween. A first helical groove is formed in at least a portion of the outer surface of the main handle and a first trigger wire actuation mechanism disposed about the main handle and rotatably moveable relative to the main handle. A first trigger wire is operatively connected to the first trigger wire actuation mechanism, the first trigger wire having a prosthesis capture condition and a prosthesis release condition. Movement of the first trigger wire actuation mechanism causes movement of the first trigger wire thereby moving the first trigger wire from the prosthesis capture condition to the prosthesis release condition. Additional trigger wire actuation mechanisms operatively connected to one or more additional trigger wires may also be disposed about the main handle.

Abstract: Valve devices, methods of making valve devices, and methods of treating various venous-related conditions, disorders and/or diseases are described. In one embodiment, a valve device includes an expandable support frame and a bioprosthetic valve attached to the support frame. The bioprosthetic valve comprises a leaflet and a contiguous wall portion harvested from a multi-leaflet xenogeneic valve. The contiguous wall portion includes the attachment region where the leaflets attaches to the vessel wall and, in some embodiments, includes the natural margins of attachment between the leaflet and vessel wall.

Abstract: A delivery system for a stent graft may include a stent graft having a proximal end, a distal end, an internal lumen between the proximal end and the distal end, a graft material tube, a graft material sidewall and a plurality of longitudinally spaced apart self-expanding stents attached to the graft material sidewall; a guidewire catheter extending longitudinally through the lumen of the stent graft; and a wire extending longitudinally along only a first side of the graft material tube in an undulating pattern of successive curves in alternate directions, the wire repeatedly extending through the graft material sidewall from inside the graft material tube to outside the graft material tube such that a portion of the wire extends over the guidewire catheter along a longitudinal length of the guidewire catheter to secure the guidewire catheter at least partially to an internal wall of the stent graft.

Abstract: A scope system including a handle that may be changed from a locked configuration to an unlocked configuration by removing a removable handle lock is provided. The handle includes features for storage of a movable elongate member on the side of the handle when the handle is in the locked configuration. In the unlocked configuration, the movable elongate member can be connected to the handle to perform desired procedures.

Abstract: A device including a needle configured to measure portal pressure in a vein of a mammal and provide an indication of a measurement a diagnostic biomarker in a sample drawn from the vein before removing the needle is provided. Methods of providing medical data about a patient by use of a device are further provided.

Abstract: Delivery device assemblies useful in the delivery of implantable medical devices, such as endografts, into a vascular system are described. A delivery device has a handle having a handle body, at least one actuator mounted to the handle body for rotation about the handle body, the actuator having a follower-driver. For each actuator, at least one follower is disposed around the handle body and is configured to rotate about the handle body. A hard stop on the handle body arrests rotation of a distal most follower for each actuator. Delivery systems, methods of making a delivery device, methods of making a delivery system, and methods of delivering an implantable medical device to a point of treatment in a body lumen are also described.

Abstract: A drainage system, including a stopcock and a clip. The stopcock includes a base and a barbed adapter extending from the base. The barbed adapter includes a shaft portion and a barbed portion. The clip includes a first grip and a second grip. The clip is configured to secure at least one tubing to the stopcock.

Abstract: The present invention relates to an introducer assembly. The introducer assembly includes a sheath and a hub assembly interconnected with the proximal end of the sheath, the hub assembly including a body defining an interior passageway in fluid communication with the lumen of the sheath, the body having a proximal end and a distal end. A valve assembly is positioned within the interior passageway of the body, the valve assembly having a valve member, the valve member being at least partially movable from a first position to a second position with respect to the valve collar. A vacuum chamber positioned distal to the valve assembly and in fluid communication with the interior passageway of the body and the lumen of the sheath, the vacuum chamber including a vacuum port.

Abstract: A stent-graft comprises: a graft defining an elongate lumen having a longitudinal axis; an external stent having a plurality of struts and apices between the struts, the apices including proximal apices and distal apices; a set of proximal sutured knots, the proximal sutured knots securing the proximal apices of the stent to the graft; a set of distal sutured knots, the distal sutured knots securing the distal apices of the stent to the graft; and a plurality of intermediate sutured knots, formed along a continuous suture, the continuous suture including a plurality of bridging portions, the bridging portions bridging between neighbouring struts of the stent, the intermediate sutured knots securing struts of the stent to the graft.

Abstract: An embolic coil delivery system includes a delivery shaft that defines a delivery shaft lumen and an embolic coil device that is detachably connected to a distal region of the delivery shaft. The embolic coil device includes coil windings that define a coil lumen. A pull wire is positioned at least partially within the delivery shaft lumen and at least partially within the coil lumen. The pull wire includes a frangible segment that is positioned within the coil lumen. The frangible segment of the pull wire defines a predictable region of separation of the pull wire in response to tensile force so as to detach said embolic coil device from said delivery shaft.

Abstract: The present embodiments provide systems and methods suitable for delivering a therapeutic agent to a target site. In some embodiments, the system comprises a container for holding the therapeutic agent, a pressure source, and a catheter in fluid communication with the container. In one embodiment, the system further comprises a first inlet tube disposed at least partially within the container, and a second inlet tube disposed at least partially within the container at a location different than the first inlet tube. Pressurized fluid from the pressure source flows into the container via each of the first inlet tube and the second inlet tube. In other embodiments, a plate is disposed with the container, wherein the plate is able to move vertically within the container during delivery of the therapeutic agent.

Abstract: Disclosed is a false lumen closure assembly for closing a false lumen in a body vessel including a compressed false lumen occluder, a carrier catheter and a retractable sheath. The compressed false lumen occluder includes a stent graft including at least one occlusive barrier across the stent graft to occlude blood flow through an interior of the stent graft. The carrier catheter carries the false lumen occluder and extends from a proximal end proximal of the false lumen occluder to a distal end distal of the false lumen occluder, and passes the false lumen occluder exteriorly of the stent graft. The compressed false lumen occluder and at least part of the carrier catheter are disposed in a lumen of the retractable sheath.

Abstract: Medical device loading apparatuses, systems, methods and kits are described. A loading apparatus comprises a main body having a passageway. The passageway has a first inner diameter, a second inner diameter, and a transition chamber. An expandable intraluminal medical device can be loaded into a delivery catheter using the loading apparatus by placing the device into the passageway and pushing the device along an axial path.

Abstract: Disclosed is a stent graft, including a graft body, a sealing stent at the proximal end of the graft body and completely overlapped by the graft body, and a diameter reducing loop arrangement. The sealing stent includes proximal apices at a proximal end thereof and distal apices at a distal end thereof. The diameter reducing loop arrangement includes a loop element. The loop element includes a first end, a second end, and a strand section from the first end to the second end. The first end is attached to the distal end of the sealing stent. The loop element is configured to pass circumferentially around the distal end of the sealing stent and have a release wire pass through a loop at the second end. The diameter reducing loop arrangement is configured to constrict the distal apices of the sealing stent and cause the sealing stent to adopt a substantially conical or frustoconical shape.

Abstract: Medical device loading apparatuses, systems, methods and kits are described. A loading apparatus comprises a main body having a passageway. The passageway has a first inner diameter, a second inner diameter, and a transition chamber. An expandable intraluminal medical device can be loaded into a delivery catheter using the loading apparatus by placing the device into the passageway and pushing the device along an axial path.

Abstract: An endoluminal graft includes a tubular graft material having a closed sleeve integral with the tubular graft material. The closed sleeve extends a distance along the tubular graft material. A length of wire extends at least partially along the distance and is enclosed by the sleeve. The tubular graft material and the sleeve may comprise a single piece of graft material. The sleeve may be a closed circumferential sleeve and/or a closed longitudinal sleeve.