Abstract: A balloon folding system specifically configured to reduce a side branch balloon of a bifurcated balloon catheter assembly includes a die that defines at least one chamber for receipt of the sidebranch balloon, and at least one pin sized to fit into the chamber and reduce the balloon to a substantially flattened state. The system also may include a housing for the reduction and folding of a primary branch balloon. The system is configurable to fold and reduce both branches simultaneously or separately.

Abstract: An expandable medical balloon having at least one static state, at least one expanded state, and at least one deflated state, the expandable medical balloon including at least one active region, the at least one active region including electroactive polymer.

Abstract: An expandable medical balloon having at least one static state, at least one expanded state, and at least one deflated state, the expandable medical balloon including at least one active region, the at least one active region including electroactive polymer.

Abstract: An occlusion device is described and depicted for occluding a body lumen. The device can comprise an occluding body member and one or more protruding portions or members disposed on the body member such that the protruding portion is provided with spacing, or surface area, to allow for tissue in-growth. The device can also comprise an expandable plug. The expandable plug may be twisted or otherwise formed into a shape, e.g., helical, in its initial deployment configuration, and untwist upon deployment.

Abstract: A method of producing a tubular member which includes providing at least one micro-extruder configured to extrude at least one material and providing a surface configured to accept the material extruded from the micro-extruder.

Abstract: An expandable medical balloon having at least one static state, at least one expanded state, and at least one deflated state, the expandable medical balloon including at least one active region, the at least one active region including electroactive polymer.

Abstract: A medical device may be secured to a medical device delivery apparatus by providing a wrapped medical device, the wrapped medical device comprising a medical device with a polymeric sheet disposed thereabout, compressing the wrapped medical device and affixing at least one opposing edge of the polymeric sheet to a portion of the polymeric sheet adjacent thereto so as to form a sheathed medical device and securing the sheathed medical device to a medical device delivery apparatus.

Abstract: A catheter comprising an outer shaft comprising a first section of electroactive polymer. The first section of electroactive polymer affecting either the flexibility of the catheter or the steerability of the catheter.

Abstract: The present invention is directed to an intracorporeal occlusion device having denuding elements, motion transfer converter or anti-migration features or a combination of one or more of these features. The disclosed occlusion device can denude the body lumen through a rotational motion of the denuding elements within a lumen. The delivery system can transfer a linear motion of a handle to a combination of linear and rotational movements of the occlusion device for placement and denuding action. Anti-migration features provide free spinning of the main body of the occlusion device to prevent migration of the deployed occlusion device, especially with rotatable denuding elements.

Abstract: A catheter assembly comprises a catheter, a rotatable sheath, a guidewire housing and a stent. The rotatable sheath is disposed about at least a portion of the catheter shaft and is rotatable thereabout. The stent is disposed about a stent receiving region of the rotatable sheath and at least a portion of the guidewire housing. The first end of the rotatable sheath extends beyond a proximal end region of the stent and the second end region of the rotatable sheath extends beyond a distal end region of the stent.

Abstract: A post dilatation balloon catheter includes a balloon member having a proximal portion, a distal portion and a circumferential bulge portion. The circumferential bulge portion extends around a circumference of the balloon member and is positioned at a location between the proximal and distal portions of the balloon member. The circumferential bulge portion inflates to a maximum inflated dimension that is greater than a maximum dimension of the proximal and distal portions of the balloon member. The balloon member is arranged into a folded state by folding at least one of the distal and proximal portions of the balloon member in a separate step from folding the circumferential bulge portion.

Abstract: Medical devices having electrically conductive pathways are disclosed. More particularly, the disclosure is directed to catheter shafts including an electrically conductive wire embedded in a polymeric tube. The disclosure is also directed to catheter shafts including an electrically conductive media coextruded in a polymeric tube. The disclosure is also directed to catheter shafts including electrically conductive pathways formed with electrically conductive ink, paste, adhesive and/or epoxy.

Abstract: In accordance with one aspect, the invention relates to medical devices which comprise at least one reservoir, a therapeutic-agent-containing region disposed within the reservoir and an electrode comprising a conductive polymer. The devices of the invention are configured such that a rate of release of the therapeutic agent from the reservoir changes upon a change in the oxidation state of the conductive polymer.

Abstract: A catheter assembly adapted to treat a vessel bifurcation. A balloon member of the catheter assembly includes a main body portion and a cylindrical shaped bulge portion that extends radially outward from the main body portion. The bulge portion extends around a circumference of the main body portion. A stent of the catheter assembly is typically mounted to the balloon member. When treating the vessel bifurcation, the catheter assembly is positioned with the bulge portion aligned axially relative to an ostium of the branch vessel. The balloon member is inflated to expand a portion of the stent into the branch vessel. The circumferential construction of the bulge portion of the balloon member reduces the need for radial (rotational) alignment of the balloon member relative to the ostium of the branch vessel.

Abstract: A catheter assembly includes a balloon member and a balloon restricting arrangement. The balloon member includes a proximal portion, a distal portion and a circumferential bulge portion. The circumferential bulge portion extends around a circumference of the balloon member and is positioned at a location between the proximal and distal portions of the balloon member. The balloon restricting arrangement includes a proximal portion extending around the proximal portion of the balloon member and a distal portion extending around the distal portion of the balloon member to restrict an inflated size of the proximal and distal portions of the balloon member. The proximal and distal portions of the balloon restricting arrangement are spaced apart axially, and the circumferential bulge portion extends radially outward therebetween.

Abstract: A balloon folding system specifically configured to reduce a side branch balloon of a bifurcated balloon catheter assembly includes a die that defines at least one chamber for receipt of the sidebranch balloon, and at least one pin sized to fit into the chamber and reduce the balloon to a substantially flattened state. The system also may include a housing for the reduction and folding of a primary branch balloon. The system is configurable to fold and reduce both branches simultaneously or separately.

Abstract: An expandable medical balloon having at least one static state, at least one expanded state, and at least one deflated state, the expandable medical balloon including at least one active region, the at least one active region including electroactive polymer.

Abstract: The present disclosure relates generally to devices, systems and methods for use with cardiac defects. A closure device includes an elongate body with a first actuator segment and a second actuator segment associated with the elongate body that can be bent into a first predetermined position and then to a second predetermined position where the distal end and the proximal end are more closely positioned than when in the first predetermined position.

Abstract: The present disclosure relates generally to devices and methods for use with cardiac defects, more particularly, the present disclosure relates to a device including a frame defining a lumen, where the frame expands from a first configuration to a second configuration larger than the first configuration. The device also includes an anchoring member extending from the frame to secure the frame while in the second configuration and a plug portion of the frame to occlude at least a portion of the lumen.

Abstract: A catheter system comprises a catheter comprising a distal portion, a proximal portion and an inner shaft. The inner shaft comprises a medical device receiving region for receiving and carrying a medical device. The retaining device is at least partially constructed of an electroactive polymer. The retaining device is located on or adjacent to the medical device receiving region. The electroactive polymer of the retaining device has an activated state and an inactivated state. The retaining device is capable of retaining a medical device to the catheter and releasing the medical device from the catheter by transitioning between the activated state and the inactivated state.