Hybrid stent having a fiber or wire backbone
    12.
    发明公开
    Hybrid stent having a fiber or wire backbone 审中-公开
    Hybridstent mit einem Faser-oderDrahtgerüst

    公开(公告)号:EP2226084A1

    公开(公告)日:2010-09-08

    申请号:EP10004585.5

    申请日:2008-03-26

    申请人: Medinol. LTD.

    发明人: Richter, Jacob

    摘要: A stent is provided with a series of short pieces or sections connected together by at least one polymer fiber or wire. The polymer fiber or wire can be biodegradable or durable. The fiber polymers may also contain beads, blobs and bulges in the fibers. The stent sections are designated to separate or articulate with time as the body lumen moves in response to biological and physiological events.

    摘要翻译: 支架设置有通过至少一种聚合物纤维或线连接在一起的一系列短片或片段。 聚合物纤维或线可以是可生物降解的或耐久的。 纤维聚合物还可以在纤维中含有珠粒,斑点和凸起。 随着体腔响应于生物和生理事件而移动,支架部分被指定为随时间分离或关节。

    HYBRID AMORPHOUS METAL ALLOY STENT
    14.
    发明公开
    HYBRID AMORPHOUS METAL ALLOY STENT 有权
    HYBRIDER STENT AUS AMORPHER METALLLEGIERUNG

    公开(公告)号:EP1996113A2

    公开(公告)日:2008-12-03

    申请号:EP07733978.6

    申请日:2007-03-14

    申请人: MEDINOL LTD.

    发明人: RICHTER, Jacob

    IPC分类号: A61F2/00

    摘要: An expandable stent is provided, wherein the stent is advantageously formed of at least one amorphous metal alloy and a biocompatible material. The stent is formed from flat metal in a helical strip which is wound to form a tubular structure. The tubular structure is not welded but rather is wrapped or coated with a biocompatible material in order to maintain the amorphous metal in its tubular configuration. Said stent can be balloon expanded or self expanding.

    摘要翻译: 提供了一种可扩张支架,其中支架有利地由至少一种非晶金属合金和生物相容性材料形成。 支架由螺旋形条中的扁平金属形成,其被卷绕以形成管状结构。 管状结构不是焊接的,而是用生物相容性材料包裹或涂覆,以便将非晶态金属保持在其管状结构中。 所述支架可以是气囊膨胀的或自膨胀的。

    A flexible expandable stent
    18.
    发明公开
    A flexible expandable stent 失效
    Flexibler,expandierbarer支架

    公开(公告)号:EP1602343A2

    公开(公告)日:2005-12-07

    申请号:EP04026188.5

    申请日:1995-07-26

    申请人: MEDINOL LTD.

    IPC分类号: A61F2/06

    摘要: There is disclosed a stent (30) for implanting in the body. The stent (30) is formed of a tube having a patterned shape which has first and second meander patterns (11, 12) having axes extending in first and second directions. The first meander patterns can be formed into even and odd first meander patterns. The even and odd first meander patterns are 180 degrees out of phase with each other, and the odd patterns occur between every two even patterns. The second meander patterns are intertwined with the first meander patterns. The first and second directions can be orthogonal to each other. The second meander patterns can also be formed of even and odd patterns.

    摘要翻译: 公开了一种用于植入体内的支架(30)。 支架(30)由具有图案形状的管形成,其具有第一和第二曲折图案(11,12),所述第一和第二曲折图案具有沿第一和第二方向延伸的轴线。 第一曲折图案可以形成为偶数和奇数的第一曲折图案。 偶数和奇数的第一曲折图案彼此相位相差180度,奇数图案出现在每两个均匀图案之间。 第二曲折图案与第一曲折图案交织在一起。 第一和第二方向可以彼此正交。 第二曲折图案也可以由均匀和奇数的图案形成。

    LONGITUDINALLY FLEXIBLE STENT
    19.
    发明公开
    LONGITUDINALLY FLEXIBLE STENT 审中-公开
    纵向柔性支架

    公开(公告)号:EP1424963A4

    公开(公告)日:2005-04-27

    申请号:EP02767765

    申请日:2002-09-06

    申请人: MEDINOL LTD

    摘要: An intravascular stent (fig. 10) especially suited for implanting in curved arterial portions. The stent (fig. 10) is formed of intertwined meander patterns forming triangular cells (804). The triangular cells (804) are adapted to provide radial support, and longitudinal flexibility after expansion. The triangular cells (804) provide increased coverage of a vessel wall. The stent (fig. 10) can have different portions adapted to optimize radial support or to optimize longitudinal flexibility. The stent (fig. 10) is curved and cells on the outside of the curve open in length, but narrow in width whereas cells on the inside of the curve shorten in length but thicken in width to maintain a density of stent element area which much more constant than otherwise between the inside and the outside of the curve. As a result, when the stent is coated with a medicine the more constant density of stent elements results in an even dose being applied to the inside wall of the lumen, avoiding the possibility that a toxic dose be supplied at one area while a less than effective dose is applied to another area.