FATIGUE RESISTANT ENDOPROSTHESES
    1.
    发明申请
    FATIGUE RESISTANT ENDOPROSTHESES 审中-公开
    耐疲劳内吞

    公开(公告)号:WO2007134321A2

    公开(公告)日:2007-11-22

    申请号:PCT/US2007/068969

    申请日:2007-05-15

    Abstract: A superelastic endoprosthesis can have improved fatigue resistance, and improved resistance to crack formation by being configuring to have an austenitic finish temperature from about 5 degrees Celsius to about 35 degrees Celsius, a stress- strain curve having an upper plateau stress from about 40 ksi to about 80 ksi, and a lower plateau stress from about 5 ksi to about 50 ksi. Such an endoprosthesis may be fabricated by heating at least a portion of the endoprosthetic body in a fluid, such as air, salt bath, or fluidized sand, having a temperature from about 400 degrees Celsius to about 600 degrees Celsius for at least about 30 seconds. Additionally, only portions of an endoprosthesis may selectively be subjected to the heating parameters of the present invention such that the endoprosthesis exhibits an increased radial stiffness and an increased flexibility in the longitudinal direction.

    Abstract translation: 超弹性内置假体可以具有改善的抗疲劳性,并且通过将奥氏体终点温度设定为约5摄氏度至约35摄氏度,具有高的平台应力约40ksi的应力 - 应变曲线 约80ksi,较低的平台压力约5ksi至约50ksi。 可以通过将具有约400摄氏度至约600摄氏度的温度的流体(例如空气,盐浴或流化砂)中的至少一部分假体内体进行加热至少约30秒来制造这种内置假体 。 此外,内部假体的仅部分可以选择性地受到本发明的加热参数的影响,使得内假体呈现出增加的径向刚度和在纵向方向上增加的柔性。

    FATIGUE RESISTANT ENDOPROSTHESES
    3.
    发明申请
    FATIGUE RESISTANT ENDOPROSTHESES 审中-公开
    耐疲劳内吞

    公开(公告)号:WO2007134321A3

    公开(公告)日:2008-03-06

    申请号:PCT/US2007068969

    申请日:2007-05-15

    Abstract: A superelastic endoprosthesis can have improved fatigue resistance, and improved resistance to crack formation by being configuring to have an austenitic finish temperature from about 5 degrees Celsius to about 35 degrees Celsius, a stress- strain curve having an upper plateau stress from about 40 ksi to about 80 ksi, and a lower plateau stress from about 5 ksi to about 50 ksi. Such an endoprosthesis may be fabricated by heating at least a portion of the endoprosthetic body in a fluid, such as air, salt bath, or fluidized sand, having a temperature from about 400 degrees Celsius to about 600 degrees Celsius for at least about 30 seconds. Additionally, only portions of an endoprosthesis may selectively be subjected to the heating parameters of the present invention such that the endoprosthesis exhibits an increased radial stiffness and an increased flexibility in the longitudinal direction.

    Abstract translation: 超弹性内置假体可以具有改善的抗疲劳性,并且通过将奥氏体终点温度设定为约5摄氏度至约35摄氏度,具有高的平台应力约40ksi至 约80ksi,较低的平台压力约5ksi至约50ksi。 可以通过将具有约400摄氏度至约600摄氏度的温度的流体(例如空气,盐浴或流化砂)中的至少一部分假体内体进行加热至少约30秒来制造这种内置假体 。 此外,内部假体的仅部分可以选择性地受到本发明的加热参数的影响,使得内假体呈现出增加的径向刚度和在纵向方向上增加的柔性。

    BODY LUMEN FILTER RETRIEVAL SYSTEM AND METHODS FOR FILTERING A BODY LUMEN
    5.
    发明申请
    BODY LUMEN FILTER RETRIEVAL SYSTEM AND METHODS FOR FILTERING A BODY LUMEN 审中-公开
    身体过滤器检索系统和过滤体液的方法

    公开(公告)号:WO2010077949A1

    公开(公告)日:2010-07-08

    申请号:PCT/US2009/068259

    申请日:2009-12-16

    Abstract: A filter retrieval system is described. The filter retrieval system may include a capture structure having an interior space bounded by an at least partially closed distal end and an open proximal end. The filter retrieval system may include an elongate retrieval member slidably disposable within at least a portion of the interior space. The elongate retrieval member may include a retrieval structure adapted to releasably engage at least a portion of a filter. Methods of using the same are disclosed.

    Abstract translation: 描述过滤器检索系统。 过滤器检索系统可以包括捕获结构,其具有由至少部分封闭的远端和敞开的近端限定的内部空间。 过滤器回收系统可以包括在内部空间的至少一部分中可滑动地一次性的细长取回构件。 细长取出构件可以包括适于可释放地接合过滤器的至少一部分的取出结构。 公开了使用该方法的方法。

    ENDOPROSTHESES FOR PERIPHERAL ARTERIES AND OTHER BODY VESSELS
    6.
    发明申请
    ENDOPROSTHESES FOR PERIPHERAL ARTERIES AND OTHER BODY VESSELS 审中-公开
    对于外围文体和其他身体的船只来说是最终的

    公开(公告)号:WO2009002631A1

    公开(公告)日:2008-12-31

    申请号:PCT/US2008/063963

    申请日:2008-05-16

    Abstract: An endoprostheses for implanting in a body lumen, such as a coronary artery, peripheral artery, or other body lumen includes a plurality of elongate strut members spaced apart and extending along a longitudinal axis, each elongate strut member having a plurality of alternating peaks and valley. At least one flexible connecting link connects each elongate strut member to an adjacent elongate strut member. The elongate strut members and connecting links forming a generally tubular stent body having a first delivery diameter and a second implanted diameter. The positioning of the connecting links along the stent body produces desired stent performance characteristics.

    Abstract translation: 用于植入体腔(例如冠状动脉,外周动脉或其他体腔)的内用假体包括间隔开并沿着纵向轴线延伸的多个细长支柱构件,每个细长的支柱构件具有多个交替的峰和谷 。 至少一个柔性连接连杆将每个细长的支柱构件连接到相邻的细长支柱构件。 细长的支柱构件和连接构件形成具有第一输送直径和第二注入直径的大体上管状的支架体。 沿着支架主体的连接件的定位产生所需的支架性能特征。

    IMPLANTABLE LUMEN FILTER WITH ENHANCED DURABILITY
    9.
    发明申请
    IMPLANTABLE LUMEN FILTER WITH ENHANCED DURABILITY 审中-公开
    具有增强耐久性的可植入式过滤器

    公开(公告)号:WO2010077963A1

    公开(公告)日:2010-07-08

    申请号:PCT/US2009/068287

    申请日:2009-12-16

    Abstract: An implantable lumen filter (100) is described. The implantable lumen filter includes a proximal portion (103a) having a generally -tapered outer surface defined by a plurality of outer struts (106). The implantable lumen filter may also include a distal portion (103b) having a generally-tapered outer surface defined by a plurality of outer struts (106b) coupled together at the distal end (102b) of the distal portion. The implantable lumen filter may also include an apex (105) comprising the connection between the proximal and distal portions. The apex may define an outer dimension of the implantable lumen filter. The outer surface of the proximal portion is dimensioned to direct particulates towards the outer dimension.

    Abstract translation: 描述可植入管腔过滤器(100)。 可植入管腔过滤器包括具有由多个外支柱(106)限定的通常夹紧的外表面的近端部分(103a)。 可植入管腔过滤器还可以包括远端部分(103b),其具有由远端部分的远端(102b)处联接在一起的多个外支柱(106b)限定的大致锥形的外表面。 可植入管腔过滤器还可以包括顶端(105),其包括近端部分和远端部分之间的连接。 顶点可以限定可植入管腔滤器的外部尺寸。 近端部分的外表面的尺寸被设计成将颗粒引向外部尺寸。

    APPARATUS FOR FILTERING A BODY LUMEN
    10.
    发明申请
    APPARATUS FOR FILTERING A BODY LUMEN 审中-公开
    用于过滤身体的装置的装置

    公开(公告)号:WO2010077973A3

    公开(公告)日:2010-08-26

    申请号:PCT/US2009068301

    申请日:2009-12-16

    Abstract: An implantable lumen filter (200) is described. The implantable lumen filter includes a body (202) having a proximal end (202a), a distal end (202b), and a generally tapered outer surface (204). The outer surface is formed by a plurality of struts (206a, 206b). The plurality of struts forms a plurality of apertures (210). The apertures are dimensioned to inhibit and/or to lyse particulates of a selected size from passing through the apertures. The body (202) is transitionable from a collapsed state toward a deployed state. The implantable lumen filter includes an engaging portion (220) having a proximal end (220a) and a distal end (220b). The proximal end of the engaging portion is connected to a distal end of the body. The engaging portion has a generally annular shape and is configured to engage an inner surface of a body lumen.

    Abstract translation: 描述可植入管腔过滤器(200)。 可植入管腔过滤器包括具有近端(202a),远端(202b)和大致锥形的外表面(204)的主体(202)。 外表面由多个支柱(206a,206b)形成。 多个支柱形成多个孔(210)。 孔的尺寸被设计成抑制和/或裂解选定尺寸的颗粒通过孔。 主体(202)可以从折叠状态向展开状态转换。 可植入管腔过滤器包括具有近端(220a)和远端(220b)的接合部分(220)。 接合部分的近端连接到主体的远端。 接合部分具有大致环形的形状并且构造成接合体腔的内表面。

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