-
公开(公告)号：US5824037A
公开(公告)日：1998-10-20
申请号：US538706
申请日：1995-10-03
申请人： Thomas J. Fogarty , Kirsten Freislinger , Steven Weinberg , Brian J. Cox , Michael A. Evans , Steven W. Kim , Jay A. Lenker
发明人： Thomas J. Fogarty , Kirsten Freislinger , Steven Weinberg , Brian J. Cox , Michael A. Evans , Steven W. Kim , Jay A. Lenker
CPC分类号： A61F2/90 , A61F2/07 , A61F2/915 , A61F2/89 , A61F2002/065 , A61F2002/075 , A61F2002/3008 , A61F2002/30199 , A61F2002/30617 , A61F2002/91591 , A61F2220/0016 , A61F2220/0041 , A61F2220/005 , A61F2220/0058 , A61F2220/0075 , A61F2230/001 , A61F2230/0054 , A61F2230/0063 , A61F2230/0067 , A61F2230/0078 , A61F2250/0097 , A61F2250/0098
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，径向适应性，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。
-
公开(公告)号：US4483023A
公开(公告)日：1984-11-20
申请号：US295160
申请日：1981-08-21
CPC分类号： A61F2/08 , A61L27/18 , A61L2430/10
摘要： A high-strength ligament prosthesis having biological acceptability, flexibility, porosity and resistance to prolonged stress in excess of 100 Kg with little change in modulus, and less than 20% ultimate elongation is provided. These characteristics make the high-strength prosthesis favorable for critical applications, such as knee and ankle repair. The high-strength prosthesis is constructed of a biological compatible yarn having an outer shell with an "H-beam" cross-section and a velour surface to encourage rapid invasion by host tissue and a reinforcing core of the same yarn. The ends of the reinforcing core and outer wall are fitted with end tips to limit displacement of the core within the outer shell and to facilitate positioning of the prosthesis during surgery with minimal effort. An enlarged elongated end tip is particularly well adapted for special surgical procedures, such as arthoscopic procedures.
摘要翻译： 提供了具有生物可接受性，柔韧性，孔隙率和抗超过100Kg的超过100Kg，几乎没有模量变化和小于20％极限伸长的高强度韧带假体。 这些特征使得高强度假体对关键应用有利，例如膝盖和踝关节修复。 高强度假体由具有“H型梁”横截面的外壳和丝锥表面的生物相容性纱线构成，以促进宿主组织的快速侵入和相同纱线的加强芯。 加强芯和外壁的端部装配有端尖以限制芯在外壳内的位移，并且有助于在手术期间以最小的努力定位假体。 扩大的细长末端特别适用于特殊的外科手术，如美术术。
-
公开(公告)号：US08627708B2
公开(公告)日：2014-01-14
申请号：US12718316
申请日：2010-03-05
IPC分类号： G01M3/02
CPC分类号： A61B19/46 , A61B90/06 , A61F2/2472 , G01M99/007 , G01N3/32 , G01N2203/0089 , G01N2203/0204 , G01N2203/0246 , G01N2203/0476
摘要： A fatigue testing system provides simultaneous cycle testing for a plurality of prosthetic devices under simulated physiological loading conditions. A plurality of sample holders containing test samples of prosthetic devices is positioned between a distribution chamber and a return fluid chamber to form an integrated test chamber. A reciprocating linear drive motor operates a rolling bellows diaphragm to cyclically pressurize fluid within the test chamber and drive the pressurized fluid through the prosthetic devices being tested. The test chamber defines a return flow conduit in fluid communication with each of the sample holders, the return fluid chamber, and the distribution chamber. Compliance chambers and throttle valves associated with each of the sample holders regulate the pressure gradient and back pressure across the prosthetic devices being tested.
摘要翻译： 疲劳测试系统在模拟的生理负载条件下为多个假肢装置提供同时的周期测试。 包含假体装置的测试样本的多个样本保持器位于分配室和返回流体室之间，以形成集成的测试室。 往复式线性驱动马达操作滚动式波纹管隔膜以周期性地加压测试室内的流体并驱动加压流体穿过所测试的假体装置。 测试室限定与每个样品保持器，返回流体室和分配室流体连通的回流管道。 与每个样品保持器相关联的合规室和节流阀调节穿过所测试的假体装置的压力梯度和背压。
-
公开(公告)号：US20120111489A1
公开(公告)日：2012-05-10
申请号：US13349803
申请日：2012-01-13
申请人： Steven Weinberg
发明人： Steven Weinberg
IPC分类号： B32B27/00
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。
-
公开(公告)号：US20110132073A1
公开(公告)日：2011-06-09
申请号：US13027507
申请日：2011-02-15
IPC分类号： G01M3/00
CPC分类号： A61B19/46 , A61B90/06 , A61F2/2472 , G01M99/007 , G01N3/32 , G01N2203/0089 , G01N2203/0204 , G01N2203/0246 , G01N2203/0476
摘要： A fatigue testing system provides simultaneous cycle testing for a plurality of prosthetic devices under simulated physiological loading conditions. A plurality of sample holders containing test samples of prosthetic devices is positioned between a distribution chamber and a return fluid chamber to form an integrated test chamber. A reciprocating linear drive motor operates a rolling bellows diaphragm to cyclically pressurize fluid within the test chamber and drive the pressurized fluid through the prosthetic devices being tested. The test chamber defines a return flow conduit in fluid communication with each of the sample holders, the return fluid chamber, and the distribution chamber. Compliance chambers and throttle valves associated with each of the sample holders regulate the pressure gradient and back pressure across the prosthetic devices being tested.
摘要翻译： 疲劳测试系统在模拟的生理负载条件下为多个假肢装置提供同时的周期测试。 包含假体装置的测试样本的多个样本保持器位于分配室和返回流体室之间，以形成集成的测试室。 往复式线性驱动马达操作滚动式波纹管隔膜以周期性地加压测试室内的流体并驱动加压流体穿过所测试的假体装置。 测试室限定与每个样品保持器，返回流体室和分配室流体连通的回流管道。 与每个样品保持器相关联的合规室和节流阀调节穿过所测试的假体装置的压力梯度和背压。
-
公开(公告)号：US20100225478A1
公开(公告)日：2010-09-09
申请号：US12718316
申请日：2010-03-05
CPC分类号： A61B19/46 , A61B90/06 , A61F2/2472 , G01M99/007 , G01N3/32 , G01N2203/0089 , G01N2203/0204 , G01N2203/0246 , G01N2203/0476
摘要： A fatigue testing system provides simultaneous cycle testing for a plurality of prosthetic devices under simulated physiological loading conditions. A plurality of sample holders containing test samples of prosthetic devices is positioned between a distribution chamber and a return fluid chamber to form an integrated test chamber. A reciprocating linear drive motor operates a rolling bellows diaphragm to cyclically pressurize fluid within the test chamber and drive the pressurized fluid through the prosthetic devices being tested. The test chamber defines a return flow conduit in fluid communication with each of the sample holders, the return fluid chamber, and the distribution chamber. Compliance chambers and throttle valves associated with each of the sample holders regulate the pressure gradient and back pressure across the prosthetic devices being tested.
摘要翻译： 疲劳测试系统在模拟的生理负载条件下为多个假肢装置提供同时的周期测试。 包含假体装置的测试样本的多个样本保持器位于分配室和返回流体室之间，以形成集成的测试室。 往复式线性驱动马达操作滚动式波纹管隔膜以周期性地加压测试室内的流体并驱动加压流体穿过所测试的假体装置。 测试室限定与每个样品保持器，返回流体室和分配室流体连通的回流管道。 与每个样品保持器相关联的合规室和节流阀调节穿过所测试的假体装置的压力梯度和背压。
-
公开(公告)号：US6123722A
公开(公告)日：2000-09-26
申请号：US226771
申请日：1999-01-05
申请人： Thomas J. Fogarty , Kirsten Freislinger , Steven Weinberg , Brian J. Cox , Michael A. Evans , Steven W. Kim , Jay A. Lenker
发明人： Thomas J. Fogarty , Kirsten Freislinger , Steven Weinberg , Brian J. Cox , Michael A. Evans , Steven W. Kim , Jay A. Lenker
CPC分类号： A61F2/90 , A61F2/07 , A61F2/915 , A61F2/89 , A61F2/91 , A61F2002/065 , A61F2002/075 , A61F2002/30199 , A61F2002/30329 , A61F2002/91591 , A61F2220/0016 , A61F2220/0025 , A61F2220/0041 , A61F2220/005 , A61F2220/0058 , A61F2220/0066 , A61F2220/0075 , A61F2230/0054 , A61F2230/0063 , A61F2230/0078 , Y10S623/902
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。
-
公开(公告)号：US5843158A
公开(公告)日：1998-12-01
申请号：US595944
申请日：1996-02-06
申请人： Jay A. Lenker , Brian J. Cox , Michael A. Evans , Steven Weinberg
发明人： Jay A. Lenker , Brian J. Cox , Michael A. Evans , Steven Weinberg
CPC分类号： A61F2/90 , A61F2/07 , A61F2/844 , A61F2002/072 , A61F2002/075 , A61F2220/005 , A61F2220/0058 , A61F2220/0075 , A61F2230/0054 , A61F2230/0078
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。
-
-
-
-
-
-
-
搜索结果
18 条记录 (耗时 0.024 秒)
