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    • 2. 发明申请
    • Catheter With Attached Flexible Side Sheath
    • 导管与附加弹性侧护套
    • US20120277851A1
    • 2012-11-01
    • US13534720
    • 2012-06-27
    • Gil M. VardiCharles J. DavidsonEric Williams
    • Gil M. VardiCharles J. DavidsonEric Williams
    • A61F2/82
    • A61F2/954A61F2/856A61F2/958A61F2250/006A61F2250/0097Y10S623/903
    • A method of positioning a main stent at a vessel bifurcation includes positioning a main guidewire in the main vessel; and advancing a stent delivery system to a position proximate the bifurcation. The stent delivery system includes a catheter with a flexible side sheath attached thereto and a main stent positioned over the catheter. The flexible side sheath is positioned to pass through the side opening in the main stent. The method also includes advancing a branch guidewire through the flexible side sheath and into the branch vessel; and subsequently, advancing the catheter over the main guidewire while advancing the flexible side sheath over the branch guidewire while viewing relative movement of a marker positioned on the flexible side sheath with respect to at least one marker positioned on the catheter.
    • 将主支架定位在血管分叉处的方法包括将主导丝定位在主血管中; 并将支架输送系统推进到靠近分叉的位置。 支架输送系统包括其上附着柔性侧鞘的导管和位于导管上的主支架。 柔性侧护套被定位成穿过主支架中的侧开口。 该方法还包括使分支导丝穿过柔性侧鞘并进入分支容器; 并且随后,当相对于位于导管上的至少一个标记物观察位于柔性侧护套上的标记物的相对运动时,将导管推进主导丝上,同时使柔性侧鞘超过分支导丝。
    • 3. 发明申请
    • BRANCH STENT GRAFT FOR AORTIC ANEURYSM REPAIR
    • 分支支架用于动态神经修复
    • US20120221090A1
    • 2012-08-30
    • US13465085
    • 2012-05-07
    • Yehuda G. WOLF
    • Yehuda G. WOLF
    • A61F2/84A61F2/82A61M5/00
    • A61F2/06A61F2/064A61F2/07A61F2/89A61F2/90A61F2/954A61F2002/061A61F2002/075A61F2002/821A61F2220/0075Y10S623/903
    • Described is a removable shunt adapted for deployment along a brain-supplying artery into an aorta to supply blood to the artery during deployment of a stent-graft in the aorta, the removable shunt including a stiff segment that is stiff enough to remain at least partially open when between the aorta and the stent-graft and large enough to allow sufficient blood supply to the brain during the deployment of the stent-graft; and a mechanism for facilitating safe removal of the shunt from between the stent-graft and the aorta. Also described is a method of deploying a branch stent graft having a flaring portion in a blood vessel branching at a bifurcation from an aorta to connect to an aortic stent graft deployed in the aorta across the bifurcation, a branch stent-graft useful in the method, and a delivery system useful in the method.
    • 描述了可拆卸分流器,其适于沿着供脑动脉部署到主动脉中,以在支架移植物在主动脉中展开期间向血管供应血液,所述可移除分流器包括刚性足够坚硬的段,以至少部分保持 在主动脉和支架移植物之间开放,并且足够大以在展开支架移植物期间允许足够的血液供应给大脑; 以及用于促进从支架移植物和主动脉之间的分流的安全移除的机构。 还描述了一种在分支从主动脉分支的血管中展开具有扩口部分的分支支架移植物连接到横跨分叉部分在主动脉中的主动脉支架移植物的方法,用于该方法的分支支架移植物 ,以及在该方法中有用的递送系统。
    • 8. 发明申请
    • Vascular Embolization With An Expansible Implant
    • 血管栓塞与可扩展植入物
    • US20090112250A1
    • 2009-04-30
    • US12337520
    • 2008-12-17
    • George R. Greene, JR.Robert F. RosenbluthBrian J. Cox
    • George R. Greene, JR.Robert F. RosenbluthBrian J. Cox
    • A61M29/04
    • A61L31/146A61B17/12022A61B17/12113A61B17/12186A61B17/1219A61B34/10A61B2017/00526A61B2017/1205A61F2/06A61L31/145A61L31/18A61L2430/36B33Y50/00B33Y80/00Y10S623/901Y10S623/903Y10T29/49
    • A vascular implant formed of a compressible foam material has a compressed configuration from which it is expansible into a configuration substantially conforming to the shape and size of a vascular site to be embolized. Preferably, the implant is formed of a hydrophilic, macroporous foam material, having an initial configuration of a scaled-down model of the vascular site, from which it is compressible into the compressed configuration. The implant is made by scanning the vascular site to create a digitized scan data set; using the scan data set to create a three-dimensional digitized virtual model of the vascular site; using the virtual model to create a scaled-down physical mold of the vascular site; and using the mold to create a vascular implant in the form of a scaled-down model of the vascular site. To embolize a vascular site, the implant is compressed and passed through a microcatheter, the distal end of which has been passed into a vascular site. Upon entering the vascular site, the implant expands in situ substantially to fill the vascular site. A retention element is contained within the microcatheter and has a distal end detachably connected to the implant. A flexible, tubular deployment element is used to pass the implant and the retention element through the microcatheter, and then to separate the implant from the retention element when the implant has been passed out of the microcatheter and into the vascular site.
    • 由可压缩泡沫材料形成的血管植入物具有压缩构型,其可膨胀到基本上符合要栓塞的血管部位的形状和尺寸的构造。 优选地,植入物由亲水的大孔泡沫材料形成,具有血管部位的缩小模型的初始构型,从而可压缩成压缩构型。 通过扫描血管部位来创建植入物以产生数字化的扫描数据集; 使用扫描数据集创建血管部位的三维数字化虚拟模型; 使用虚拟模型创建血管部位的缩小物理模具; 并使用模具以血管部位的缩小模型的形式产生血管植入物。 为了栓塞血管部位,植入物被压缩并通过微导管,其远端已经进入血管部位。 在进入血管部位时,植入物基本上扩张以填充血管部位。 保持元件容纳在微导管内并且具有可拆卸地连接到植入物的远端。 使用柔性的管状展开元件将植入物和保持元件通过微导管,然后当植入物从微导管通过并进入血管部位时,将植入物与保留元件分离。
    • 9. 发明授权
    • Self contracting stent
    • 自体支架
    • US07524329B2
    • 2009-04-28
    • US11348278
    • 2006-02-06
    • Brian K. Rucker
    • Brian K. Rucker
    • A61F2/06
    • C22F1/00A61F2/88A61F2/90A61F2002/9528C22F1/006Y10S623/903
    • A self-contracting stent for use at a treatment site comprising shape memory material is provided. The stent may have an initial diameter for delivery to the treatment site and an expanded diameter when deployed at the treatment site. The stent further may have a contracted diameter when subjected to a temperature at or above a transition temperature. The contracted diameter is less than the expanded diameter and permits repositioning or removal of the stent from the treatment site. Additionally, a method for delivering and recovering the stent from a treatment site is provided. The method includes delivering a stent to a treatment site and expanding the stent at the treatment site so that the stent is deployed at the treatment site. The method further includes changing the temperature of the stent at the treatment site to at least a transition temperature to cause the stent to contract.
    • 提供了一种在包括形状记忆材料的治疗部位使用的自体收缩支架。 支架可以具有用于输送到治疗部位的初始直径,并且在部署在治疗部位时具有扩大的直径。 当经受等于或高于转变温度的温度时,支架还可具有收缩直径。 收缩直径小于扩张直径,并允许支架从治疗部位重新定位或移除。 另外,提供了用于从治疗部位输送和回收支架的方法。 该方法包括将支架输送到治疗部位并在治疗部位扩张支架,使得支架部署在治疗部位。 该方法还包括将处置部位的支架的温度改变至至少转变温度以使支架收缩。