Fatigue evaluation of prostheses by radial excitation of tubular structures
    3.
    发明申请
    Fatigue evaluation of prostheses by radial excitation of tubular structures 有权
    通过管状结构的径向激发对假体的疲劳评估

    公开(公告)号:US20110146385A1

    公开(公告)日:2011-06-23

    申请号:US12975772

    申请日:2010-12-22

    IPC分类号: G01N3/32

    摘要: Prostheses are fatigue tested using an apparatus under simulated physiological loading conditions. A fluid housing defines an entrance chamber having fluid outflow ports and an exit chamber having opposing fluid inflow ports and a central flow conduit in communication with the entrance chamber and the exit chamber. A plurality of housing tubes into which prosthesis are deployed may extend between the fluid outflow and inflow ports. Alternatively, tubular prostheses may be connected directly between the inflow and outflow ports. A reciprocating linear drive pump having a flexible diaphragm is provided to cyclically pressurize fluid through a common closed loop within the fluid housing and drive the pressurized fluid through the prosthesis being tested. The test system is capable of rotation independent of the motor drive for accurate diameter measurements of all test samples at elevated frequencies.

    摘要翻译: 使用模拟生理负荷条件下的装置对假体进行疲劳试验。 流体壳体限定具有流体流出端口的入口室和具有相对的流体流入口的出口室和与入口室和出口室连通的中心流动管道。 假体部署在其中的多个外壳管可以在流体流出口和流入口之间延伸。 或者,管状假体可以直接连接在流入口和流出口之间。 提供具有柔性隔膜的往复式线性驱动泵,以通过流体外壳内的公共闭环循环地加压流体,并驱动加压流体穿过被测假体。 测试系统能够独立于电机驱动器进行旋转,以便在高频下对所有测试样品进行精确的直径测量。

    Cuffed endoluminal prosthesis
    4.
    发明授权
    Cuffed endoluminal prosthesis 有权
    袖口内腔假体

    公开(公告)号:US06592614B2

    公开(公告)日:2003-07-15

    申请号:US09726431

    申请日:2000-12-01

    IPC分类号: A61F206

    摘要: The present invention provides controlled expansion endoluminal prostheses and methods for their deployment and expansion. The present stent-grafts generally comprise a radially expansible tubular frame and a plastically expansible liner on the frame. Either the frame or the liner includes a reinforcing element which limits expansion of the stent-graft at a predetermined expanded size. In some embodiments, the reinforcing element restrains the frame, for example, by limiting the circumferential diagonals of perforations on a perforate frame structure. Generally, however, the reinforcing element is included in the liner as circumferentially oriented yarn. A particularly advantageous liner includes composite circumferential yarns having inexpansible fibers wrapped around an expansible fiber, such as a partially oriented yarn, PTFE, or the like.

    摘要翻译: 本发明提供受控的扩张腔内假体及其部署和扩张的方法。 本发明的支架移植物通常包括径向可膨胀的管状框架和框架上的塑性可膨胀的衬垫。 框架或衬里都包括限制扩张器移植物以预定的扩大尺寸的扩张的增强元件。 在一些实施例中,增强元件例如通过限制穿孔框架结构上的穿孔的周向对角线来限制框架。 然而,通常,增强元件作为圆周取向的纱线包括在衬套中。 特别有利的衬里包括具有缠绕在可膨胀纤维(例如部分取向纱线,PTFE等)上的不可消耗纤维的复合周向纱线。

    Fatigue evaluation of prostheses by radial excitation of tubular structures
    5.
    发明授权
    Fatigue evaluation of prostheses by radial excitation of tubular structures 有权
    通过管状结构的径向激发对假体的疲劳评估

    公开(公告)号:US08490504B2

    公开(公告)日:2013-07-23

    申请号:US12975772

    申请日:2010-12-22

    IPC分类号: G01N3/36

    摘要: Prostheses are fatigue tested using an apparatus under simulated physiological loading conditions. A fluid housing defines an entrance chamber having fluid outflow ports and an exit chamber having opposing fluid inflow ports and a central flow conduit in communication with the entrance chamber and the exit chamber. A plurality of housing tubes into which prosthesis are deployed may extend between the fluid outflow and inflow ports. Alternatively, tubular prostheses may be connected directly between the inflow and outflow ports. A reciprocating linear drive pump having a flexible diaphragm is provided to cyclically pressurize fluid through a common closed loop within the fluid housing and drive the pressurized fluid through the prosthesis being tested. The test system is capable of rotation independent of the motor drive for accurate diameter measurements of all test samples at elevated frequencies.

    摘要翻译: 使用模拟生理负荷条件下的装置对假体进行疲劳试验。 流体壳体限定具有流体流出端口的入口室和具有相对的流体流入口的出口室和与入口室和出口室连通的中心流动管道。 假体部署在其中的多个外壳管可以在流体流出口和流入口之间延伸。 或者,管状假体可以直接连接在流入口和流出口之间。 提供具有柔性隔膜的往复式线性驱动泵,以通过流体外壳内的公共闭环循环地加压流体,并驱动加压流体穿过被测假体。 测试系统能够独立于电机驱动器进行旋转,以便在高频下对所有测试样品进行精确的直径测量。

    Self-sealing vascular graft
    6.
    发明申请
    Self-sealing vascular graft 有权
    自密封血管移植

    公开(公告)号:US20070123968A1

    公开(公告)日:2007-05-31

    申请号:US11517683

    申请日:2006-09-08

    申请人: Steven Weinberg

    发明人: Steven Weinberg

    IPC分类号: A61F2/06

    CPC分类号: A61M39/0208 A61M2039/0072

    摘要: The present invention relates to a segmental self-sealing graft for implantation in a patient including a base tubing element, a tubular access element overlying the base tubing, and a strand-like compression element wound over the access element so as to provide radially inward compression, and a method of making same.

    摘要翻译: 本发明涉及用于植入患者的分段自密封移植物,包括基管元件,覆盖基管的管状进入元件和缠绕在进入元件上的股线状压缩元件,以便提供径向向内的压缩 ,及其制作方法。

    Self-sealing vascular graft
    7.
    发明授权
    Self-sealing vascular graft 有权
    自密封血管移植

    公开(公告)号:US08163002B2

    公开(公告)日:2012-04-24

    申请号:US11517683

    申请日:2006-09-08

    申请人: Steven Weinberg

    发明人: Steven Weinberg

    IPC分类号: A61F2/06

    CPC分类号: A61M39/0208 A61M2039/0072

    摘要: The present invention relates to a segmental self-sealing graft for implantation in a patient including a base tubing element, a tubular access element overlying the base tubing, and a strand-like compression element wound over the access element so as to provide radially inward compression, and a method of making same.

    摘要翻译: 本发明涉及用于植入患者的分段自密封移植物,包括基管元件,覆盖基管的管状进入元件和缠绕在进入元件上的股线状压缩元件,以便提供径向向内的压缩 ,及其制作方法。

    Glass
    8.
    外观设计
    Glass 失效
    玻璃

    公开(公告)号:USD452634S1

    公开(公告)日:2002-01-01

    申请号:US29132806

    申请日:2000-11-17

    申请人: Steven Weinberg

    设计人: Steven Weinberg

    Modular intraluminal prosteheses construction and methods
    9.
    发明授权
    Modular intraluminal prosteheses construction and methods 失效
    模块性腔内工程施工及方法

    公开(公告)号:US06193745B1

    公开(公告)日:2001-02-27

    申请号:US08868902

    申请日:1997-06-04

    IPC分类号: A61F204

    摘要: The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or “prosthetic modules,” may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.

    摘要翻译: 本发明提供了用于治疗疾病状况,特别是动脉瘤的模块化管腔内管状假体,特别是支架和支架移植物。 可以选择性地组合假体的模块化部分或“假体模块”,以形成具有根据患者的具体要求定制的特征的复合假体。 每个假体模块优选地包括用于接合另一模块的一个或多个标准接口端,模块/模块接口通常包括在预定轴向范围内重叠和/或锁定的端部。 有利地,可以沿着复合假体的轴线改变轴向长度,横截面,周长,弹性膨胀力,轴向柔性,衬垫渗透性,衬垫延伸性,径向顺应性,衬垫/输卵管壁密封和锚定以及其他假体特征 ,并且还沿着每个假体模块的轴线。 模块优选地单独地引入到患者体的管腔系统中,使得复合假体原位组装。 理想地,合适的假体模块的选择以及界面重叠范围的灵活性提供了一种定制适合的腔内假体,其提供针对个体患者需要的治疗。

    Method for deploying cuff prostheses
    10.
    发明授权
    Method for deploying cuff prostheses 有权
    部署袖口假体的方法

    公开(公告)号:US6110198A

    公开(公告)日:2000-08-29

    申请号:US225992

    申请日:1999-01-05

    摘要: The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or "prosthetic modules," may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module/module interface typically comprising ends which overlap and/or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner/tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.

    摘要翻译: 本发明提供了用于治疗疾病状况,特别是动脉瘤的模块化管腔内管状假体,特别是支架和支架移植物。 可以选择性地组合假体的模块化部分或“假体模块”,以形成具有根据患者的具体要求定制的特征的复合假体。 每个假体模块优选地包括用于接合另一模块的一个或多个标准接口端,模块/模块接口通常包括在预定轴向范围内重叠和/或锁定的端部。 有利地,可以沿着复合假体的轴线改变轴向长度,横截面,周长,弹性膨胀力,轴向柔性,衬垫渗透性,衬垫延伸性,径向顺应性,衬垫/输卵管壁密封和锚定以及其他假体特征 ,并且还沿着每个假体模块的轴线。 模块优选地单独地引入到患者体的管腔系统中,使得复合假体原位组装。 理想地,合适的假体模块的选择以及界面重叠范围的灵活性提供了一种定制适合的腔内假体,其提供针对个体患者需要的治疗。