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    • 3. 发明授权
    • Stent with dual support structure
    • 支架双支撑结构
    • US08900289B2
    • 2014-12-02
    • US13198770
    • 2011-08-05
    • Paul J. Thompson
    • Paul J. Thompson
    • A61F2/06A61F2/91A61F2/915
    • A61F2/86A61F2/91A61F2/915A61F2002/91508A61F2002/91525A61F2002/91541A61F2002/91558A61F2002/91566A61F2230/0013A61F2230/0054A61F2250/001
    • A intraluminal stent comprises a reticulated tube having an un-deployed diameter and expandable to an enlarged diameter. The tube includes a structural beam extending between first and second ends. The structural beam changes from a first geometry to a second geometry when the tube changes from the un-deployed diameter to the enlarged diameter. The structural beam includes first and second longitudinal elements each extending at least partially between the first and second ends and with a spacing between the first and second elements. Each of said first and second elements changes from the first geometry to the second geometry when the tube changes from the un-deployed diameter to the enlarged diameter for the spacing to remain substantially unchanged as the tube changes from the un-deployed diameter to the enlarged diameter.
    • 管腔内支架包括具有未展开直径并且可扩张至扩大直径的网状管。 管包括在第一和第二端之间延伸的结构梁。 当管从未展开的直径变大到扩大的直径时,结构梁从第一几何变化到第二几何形状。 结构梁包括第一和第二纵向元件,每个第一和第二纵向元件至少部分地在第一和第二端之间延伸并且在第一和第二元件之间具有间隔。 当管从未展开的直径改变到扩大的直径时,所述第一和第二元件中的每一个从第一几何形状变化到第二几何形状,以使间隔保持基本上不变,因为管从未展开的直径变大到扩大的直径 直径。
    • 6. 发明申请
    • EXPANDABLE PYLORIC ANCHORS AND METHODS FOR SECURING INTESTINAL BYPASS SLEEVES
    • 可扩展的PYLORIC锚杆及其安装方法
    • US20120065571A1
    • 2012-03-15
    • US13298867
    • 2011-11-17
    • Paul J. ThompsonKedar R. BelheAlex Grafov
    • Paul J. ThompsonKedar R. BelheAlex Grafov
    • A61M5/00
    • A61F5/0076A61F5/0079A61F2002/044A61F2002/045
    • A gastrointestinal device for implanting within a patient's gastrointestinal tract includes first and second expandable anchoring rings configured to be disposed on either side of a patient's pylorus. The first expandable anchoring ring has a collapsed configuration and an expanded configuration, wherein in the expanded configuration the first expandable anchoring ring has a diameter larger than a maximum opening diameter of the pylorus. The second expandable anchoring ring also has a collapsed configuration and an expanded configuration, wherein in the expanded configuration the second expandable anchoring ring has a diameter larger than a maximum opening diameter of the pylorus. An intestinal bypass sleeve couples the first expandable anchoring ring and the second expandable anchoring ring, so as to allow a distance between the anchoring rings to exceed a width of the pylorus.
    • 用于植入患者胃肠道内的胃肠装置包括被配置为设置在患者幽门的任一侧上的第一和第二可扩张锚定环。 第一可膨胀锚固环具有收缩构型和膨胀构型,其中在膨胀构型中,第一可膨胀锚定环的直径大于幽门的最大开口直径。 第二可膨胀锚固环还具有收缩构型和膨胀构型,其中在膨胀构型中,第二可膨胀锚定环的直径大于幽门的最大开口直径。 肠旁路套管将第一可膨胀锚固环和第二可膨胀锚固环联接,以便允许锚定环之间的距离超过幽门的宽度。
    • 8. 发明申请
    • STENT WITH DUAL SUPPORT STRUCTURE
    • 具有双重支持结构的STENT
    • US20100087912A1
    • 2010-04-08
    • US12633246
    • 2009-12-08
    • Paul J. Thompson
    • Paul J. Thompson
    • A61F2/82
    • A61F2/86A61F2/91A61F2/915A61F2002/91508A61F2002/91525A61F2002/91541A61F2002/91558A61F2002/91566A61F2230/0013A61F2230/0054A61F2250/001
    • A intraluminal stent comprises a reticulated tube having an un-deployed diameter and expandable to an enlarged diameter. The tube includes a structural beam extending between first and second ends. The structural beam changes from a first geometry to a second geometry when the tube changes from the un-deployed diameter to the enlarged diameter. The structural beam includes first and second longitudinal elements each extending at least partially between the first and second ends and with a spacing between the first and second elements. Each of said first and second elements changes from the first geometry to the second geometry when the tube changes from the un-deployed diameter to the enlarged diameter for the spacing to remain substantially unchanged as the tube changes from the un-deployed diameter to the enlarged diameter.
    • 管腔内支架包括具有未展开直径并且可扩张至扩大直径的网状管。 管包括在第一和第二端之间延伸的结构梁。 当管从未展开的直径变大到扩大的直径时,结构梁从第一几何变化到第二几何形状。 结构梁包括第一和第二纵向元件,每个第一和第二纵向元件至少部分地在第一和第二端之间延伸并且在第一和第二元件之间具有间隔。 当管从未展开的直径改变到扩大的直径时,所述第一和第二元件中的每一个从第一几何形状变化到第二几何形状,以使间隔保持基本上不变,因为管从未展开的直径变大到扩大的直径 直径。
    • 9. 发明申请
    • CATHETER SYSTEM WITH SPACER MEMBER
    • 带间隔器的导管系统
    • US20100082090A1
    • 2010-04-01
    • US12608159
    • 2009-10-29
    • Paul J. ThompsonRichard C. Gunderson
    • Paul J. ThompsonRichard C. Gunderson
    • A61F2/06
    • A61F2/962A61F2/95A61F2/958A61F2/966A61F2002/9505A61F2002/9517A61M25/0021A61M25/0043A61M25/0045A61M25/007
    • A stent delivery system includes outer and inner elongated, flexible tubular members each having a distal and proximal ends. The outer tubular member is sized to be passed through the body lumen with the distal end advanced to the deployment site and with the proximal end remaining external of the patient's body for manipulation by an operator. The inner tubular member is sized to be received within the outer tubular member. The inner tubular member has a stent attachment location at its distal end. A spacer member is disposed between the inner and outer tubular members. The spacer member maintains spacing between the inner and outer tubular members. Opposing surfaces of the inner and outer tubular members define a passageway extending from the proximal end towards the distal end of the outer tubular member. A fluid exchange port is provided in communication with the passageway at the proximal end of the outer tubular member.
    • 支架输送系统包括外部和内部细长的柔性管状构件,每个具有远端和近端。 外管状构件的尺寸设置成穿过身体内腔,远端前进到展开位置,并且近端保留在患者身体的外部,由操作者操纵。 内管状构件的尺寸设置成容纳在外管状构件内。 内部管状构件在其远端具有支架附接位置。 间隔构件设置在内管状构件和外管状构件之间。 隔离构件保持内管状构件和外管状构件之间的间隔。 内管状构件和外管状构件的相对表面限定了从外管状构件的近端向远端延伸的通道。 流体交换端口设置成与外管状构件的近端处的通道连通。
    • 10. 发明授权
    • Braided composite prosthesis
    • 编织复合假体
    • US07211109B2
    • 2007-05-01
    • US10775961
    • 2004-02-10
    • Paul J. Thompson
    • Paul J. Thompson
    • A61F2/06
    • D04C1/06A61B90/39A61F2/06A61F2/07A61F2/90A61F2/95A61F2002/072A61F2220/0008A61F2220/0016A61F2220/0075A61F2240/001D10B2509/06
    • A prosthesis for transluminal implantation consists of a flexible tubular interbraided structure of metal or polymeric monofilaments, and polymeric multifilament yarns. The prosthesis can be elastically deformed to reduce its diameter through axial elongation. The monofilaments and multifilament yarns are arranged in axially spaced apart helices, concentric on a common central axis of the prosthesis. The monofilaments are selectively shaped before their interbraiding with the multifilament yarns, either by an age-hardening or other heat-setting stage, or a cold-working stage that controllably plastically deforms the strands. The shaped structural strands cooperate to impart to the prosthesis its nominal shape and resilience. The textile strands cooperate to provide a sheeting that occupies interstices between adjacent structural strands, to reduce permeability and thereby enhance the utility of the prosthesis as a vascular graft. An alternative embodiment prosthesis includes elastically and plastically deformable structural strands, selectively plastically deformed by cold-working then interbraided to form the prosthesis.
    • 用于腔内植入的假体由金属或聚合单丝的柔性管状插入结构和聚合复丝纱组成。 假体可以通过轴向伸长而弹性变形以减小其直径。 单丝和复丝纱布置在轴向间隔开的螺旋中,同心于假体的共同中心轴线。 单丝在通过时效硬化或其它热定型阶段或可控地塑性地使股线变形的冷加工阶段之前与复丝纱线相互交错而选择成形。 成形的结构丝线协作以赋予假体其标称形状和弹性。 纺织品线合作提供占据相邻结构链之间间隙的片材,以减少渗透性,从而增强假体作为血管移植物的效用。 替代实施例假体包括弹性和塑性变形的结构股,通过冷加工选择性塑性变形,然后插入以形成假体。