Abstract: A catheter comprises a catheter shaft, at least a portion of which defines a medical device receiving region, and at least one sleeve. The at least one sleeve comprises a tubular member constructed and arranged to transition between an extended state and a retracted state. The tubular member has a first portion being engaged to a portion of the catheter shaft adjacent to the medical device receiving region. In the extended state a second portion is constructed and arranged to at least partially overlay the medical device receiving region. In the retraced state the second portion is removed from about the medical device receiving region. At least one of the first portion and the second portion of the tubular member are at least partially constructed from a shape memory material.

Abstract: A device for at least partially occluding an aneurysm is disclosed. The device includes a first elongate member having a distal end. A bridge is positioned proximate the distal end and transformable between a delivery configuration and a deployed configuration. A second elongate member is movable relative to the first elongate member, the first and second elongate members being configured such that one can be moved relative to the other in order to transform the bridge between the delivery and deployed configurations.

Abstract: An medical device include a shaft having an elongated inner tubular member and an elongated tubular reinforcing member disposed over a portion of the inner tubular member. In some embodiments, the reinforcing member is disposed about a proximal portion of the inner tubular member such that a distal portion of the inner tubular member is free of the reinforcing member. In some embodiments, the at least a portion of an outer surface of the inner tubular member is spaced from an inner surface of the reinforcing member. In some embodiments, the shaft can include a tip structure disposed on the distal portion of the inner tubular member. In some such embodiments, reinforcing member has a distal end, and the tip structure is disposed on the distal portion of the inner tubular member adjacent the distal end of the reinforcing member.

Abstract: A fiber optic probe of the type typically used in medical instruments includes an illumination optical fiber having a relatively high Numerical Aperture (NA) for coupling as much light as possible into the fiber at its input end. At the output end, an outwardly flared uniform taper is proved to increase coloration of the light exiting from the illumination end, thereby causing the Numerical Aperture (NA) at the output end of the illumination fiber to be a lower NA than that at the input end. Additionally, there is a bevel cut into the end of the fiber to provide total internal reflectance whereby the source light is redirected out a side of the fiber. A sidewall face may be provided to provide for a circular rather than an elliptical illumination spot.

Abstract: The present invention to is directed toward an integrated standard platform for the integration of content distributor's back office processes with multiple services from different vendors. A centralized management architecture supporting configuration and accounting management functions for multiple services is provided. The architecture comprises a database for storing configuration, user profile and usage data. The architecture also includes a service and a support gateway to regulate the provisioning, security, policies and operations regarding the content delivery. The centralized architecture has the ability to manipulate data stored in the database for facilitating delivery and control of service provided by the third party vendors. The architecture further includes a package manager module, which allows the content distributor to personalize the available content for an individual user.

Abstract: A sacrificial anode stent system comprises a stent having at least one sacrificial anode portion and a vaso-occlusive device. The vaso-occlusive device has at least one portion with a potential different from that of the sacrificial anode portion of the stent.

Abstract: An intravascular catheter including a proximal stiff metallic tube and a distal flexible tube. A distal portion of the metallic tube has a portion removed to define a void (e.g., spiral slot) which decreases the stiffness of the metallic tube. A proximal portion of the distal flexible tube is disposed in the void to provide a secure connection and to blend the stiffness of the metallic proximal tube and the flexible distal tube without significantly increasing profile.

Abstract: A catheter comprises a catheter shaft, at least a portion of which defines a medical device receiving region, and at least one sleeve. The at least one sleeve comprises a tubular member constructed and arranged to transition between an extended state and a retracted state. The tubular member has a first portion being engaged to a portion of the catheter shaft adjacent to the medical device receiving region. In the extended state a second portion is constructed and arranged to at least partially overlay the medical device receiving region. In the retraced state the second portion is removed from about the medical device receiving region. At least one of the first portion and the second portion of the tubular member are at least partially constructed from a shape memory material.

Abstract: A medical implant for implantation in a bodily vessel may comprise a tungsten-rhenium (Re) alloy. Another medical implant for implantation in a bodily vessel may comprise molybdenum TZM alloy. Another medical implant may be provided in the form of a stent manufactured from a sheet of metal or from a metal tube, the metal having a modulus of elasticity of 300 GPa or greater.

Abstract: A system and method are disclosed for preparing platens to perform lapping operations. The system includes a platter that is rotatably mounted on a base and designed to receive the platen thereon. A main drive motor is provided for rotating the platter and the platen disposed thereon. A plurality of pressure arms are disposed on the base and configured to include a tool receiving portion that can be positioned in alignment with a lapping surface of the platen, and configured to softly touch a tool to a platen. A tool is attached to each tool receiving portion so that predetermined operations can be performed on the lapping surface of the platen. A monitor is provided to monitor predetermined parameters and maintain substantially constant conditions while preparing the platen.

Abstract: A system and method are disclosed for preparing platens to perform lapping operations. The system includes a platter that is rotatably mounted on a base and designed to receive the platen thereon. A main drive motor is provided for rotating the platter and the platen disposed thereon. A plurality of pressure arms are disposed on the base and configured to include a tool receiving portion that can be positioned in alignment with a lapping surface of the platen. A tool is attached to each tool receiving portion so that predetermined operations can be performed on the lapping surface of the platen. A monitor is provided to monitor predetermined parameters and maintain substantially constant conditions while preparing the platen.

Abstract: A guidewire having a super elastic core surrounded by a shape memory polymer jacket. The super elastic core wire permits the guidewire to be navigated through tortuous vasculature without undergoing plastic deformation, and the shape memory polymer jacket permits the guidewire to be shaped by the physician.

Abstract: A guide wire with a distal portion having adjustable flexibility. The guide wire may include a distal polymeric member and a heat source. The heat source may be activated to cause the polymeric member to increase in temperature and increase in flexibility. The increase in flexibility of the distal portion of the guide wire enhances the ability of the guide wire to navigate tortuous vasculature to a target site. After the guide wire has been navigated to the target site, the heat source may be deactivated to cause the polymeric member to decrease in temperature and increase in stiffness. The increase in stiffness of the distal portion of the guide wire enhances support provided for devices (e.g., catheters) advanced thereon.

Abstract: An intravascular catheter including a proximal stiff metallic tube and a distal flexible tube. A distal portion of the metallic tube has a portion removed to define a void (e.g., spiral slot) which decreases the stiffness of the metallic tube. A proximal portion of the distal flexible tube is disposed in the void to provide a secure connection and to blend the stiffness of the metallic proximal tube and the flexible distal tube without significantly increasing profile.

Abstract: A system and method are disclosed for preparing platens to perform lapping operations. The system includes a platter that is rotatably mounted on a base and designed to receive the platen thereon. A main drive motor is provided for rotating the platter and the platen disposed thereon. A plurality of pressure arms are disposed on the base and configured to include a tool receiving portion that can be positioned in alignment with a lapping surface of the platen, and configured to softly touch a tool to a platen. A tool is attached to each tool receiving portion so that predetermined operations can be performed on the lapping surface of the platen. A monitor is provided to monitor predetermined parameters and maintain substantially constant conditions while preparing the platen.

Abstract: A fiber optic probe of the type typically used in medical instruments includes an illumination optical fiber having a relatively high Numerical Aperture (NA) for coupling as much light as possible into the fiber at its input end. At the output end, an outwardly flared uniform taper is proved to increase coloration of the light exiting from the illumination end, thereby causing the Numerical Aperture (NA) at the output end of the illumination fiber to be a lower NA than that at the input end. Additionally, there is a bevel cut into the end of the fiber to provide total internal reflectance whereby the source light is redirected out a side of the fiber. A sidewall face may be provided to provide for a circular rather than an elliptical illumination spot.

Abstract: A high energy surgical launch fiber termination includes a cylindrical quartz ferrule having a bore through it of a first predetermined diameter. An optical fiber, which has at least a silica core and a polymer external jacket, is attached to the quartz ferrule by stripping the external jacket from a length of the end of the optical fiber to expose a portion of the silica core. This inner core is inserted into the bore in the quartz ferrule, and is fused to the ferrule by means of heat fusion, without employing any adhesives, to bond the ferrule and the optical fiber together. A metal beam block surrounds at least a portion of the quartz ferrule on the side where the optical fiber is inserted into it. The beam block includes an extension surrounding the polymer external jacket of the fiber; and the extension is crimped onto the polymer jacket to hold the beam block and fiber in place.

Abstract: A fiber optic probe of the type typically used in medical instruments includes an illumination optical fiber having a relatively high Numerical Aperture (NA) for coupling as much light as possible into the fiber at its input end. At the output end, an outwardly flared uniform taper is provided to increase collimation of the light exiting from the illumination end, thereby causing the Numerical Aperture (NA) at the output end of the illumination fiber to be a lower NA than that at the input end. For optical spectroscopy applications, collection fibers are located in close proximity to or surrounding the tapered output end of the illumination fiber for collecting reflected or scattered light rays from a target for use in qualitative and quantitative analysis of material.