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    • 52. 发明授权
    • Ultrasonic angioplasty transmission member
    • 超声波血管成形术传播部件
    • US06494891B1
    • 2002-12-17
    • US09474953
    • 1999-12-30
    • Wayne E. CornishRobert C. EsselsteinSepehr FariabiHenry Nita
    • Wayne E. CornishRobert C. EsselsteinSepehr FariabiHenry Nita
    • A61B1732
    • A61B17/22012A61B2017/22015A61B2017/22018
    • The ultrasonic angioplasty transmission wire has regions of reduced cross-sectional diameter to improve flexibility of the ultrasonic angioplasty transmission wire and to compensate for degradation of longitudinal displacement due to acoustic losses along the length of the ultrasonic angioplasty transmission wire. One or more constraining members are disposed on the ultrasonic angioplasty transmission wire at one or more of the regions of reduced cross-sectional diameter where transverse vibration of ultrasonic energy transmitted by the ultrasound transmission wire is amplified, to constrain transverse vibration at these areas to reduce stress and reduce fracturing, while allowing longitudinal movement. The transmission wire has an elongated shaft including, in atomic percent, from about 28 to about 52 percent nickel, from about 48 to about 52 percent titanium, and up to about 20 percent of at least one alloying element selected from the group consisting of palladium, chromium, and hafnium.
    • 超声波血管成形术传输线具有减小的横截面直径的区域,以改善超声波血管成形术传输线的柔性,并且补偿由于沿着超声波血管成形术传输线的长度的声学损失引起的纵向位移的退化。 一个或多个约束构件设置在超声波血管成形术传输线上的一个或多个减小横截面直径的区域中,其中由超声波传输线传输的超声能量的横向振动被放大,以限制这些区域的横向振动,以减少 应力和减少压裂,同时允许纵向移动。 传输线具有细长轴,原子百分比包括约28至约52%的镍,约48至约52%的钛,以及至多一种选自钯的至少一种合金元素的至多约20% ,铬和铪。
    • 55. 发明授权
    • Nickel-titanium core guide wire
    • 镍钛芯导丝
    • US08500658B2
    • 2013-08-06
    • US12914049
    • 2010-10-28
    • William J. BoyleWayne E. CornishRaleigh A. Purtzer
    • William J. BoyleWayne E. CornishRaleigh A. Purtzer
    • A61B5/00
    • A61M25/09A61M2025/09175Y10T29/49986Y10T29/5187
    • A guide wire for use in a medical procedure having a shapeable tip integral with and made from the distal end of a superelastic nitinol distal section of the guide wire, wherein the shapeable tip can be finger kinked. Such a guide wire includes an elongated core made from a superelastic nitinol alloy at the distal end, the distal end of the elongated core having a tapered section leading to a shapeable distal tip. The shapeable tip is an extension of the distal end of the nitinol distal section, and includes permanent strain hardening from at least two different radial directions imparting crystallographic texture in the radial directions that eliminate superelasticity so that permanent deformation can be achieved with finger pressure.
    • 一种用于医疗过程的导丝,其具有与引导线的超弹性镍钛诺远端部分的远端一体并由远端制成的可成形尖端,其中可成形尖端可以被扭曲。 这种导丝包括在远端由超弹性镍钛诺合金制成的细长芯,细长芯的远端具有通向可成形的远端的锥形部分。 可成形尖端是镍钛诺骨远端部分的远端的延伸部,并且包括从至少两个不同径向方向的永久性应变硬化,其赋予径向方向上的结晶学结构,从而消除超弹性,从而可以用手指压力实现永久变形。
    • 57. 发明授权
    • Guide wire with embolic filtering attachment
    • 导丝与栓塞过滤附件
    • US07815660B2
    • 2010-10-19
    • US12025404
    • 2008-02-04
    • Douglas H. GessweinWayne E. CornishScott J. HuterBenjamin C. HuterJohn E. Papp
    • Douglas H. GessweinWayne E. CornishScott J. HuterBenjamin C. HuterJohn E. Papp
    • A61M29/00
    • A61F2/013A61F2002/018A61F2230/0006A61F2230/0067A61F2230/008
    • A separate deliverable embolic protection device filter that attaches to a helical coil at a distal end of a conventional guide, for use in a blood vessel when an interventional procedure is being performed to capture any embolic material which may be created and released into the bloodstream during the procedure. The device includes a filter assembly with a proximal end and a distal end, and a guide wire connector attached to the distal end of the filter assembly. The guide wire connector is able to couple with the helical coil of the guide wire. A restraining sheath placed over the filter assembly in a coaxial arrangement maintains the filter assembly in a collapsed position and delivers the filter assembly separately to the helical coil of the guide wire, and then the guide wire connector is joined to the helical coil. Alternatively, the guide wire can include a rotatable coil section forming a portion of the distal tip coil on the guide wire which is adapted to be coupled to the filter assembly. This arrangement allows the filter assembly to be rotatably mounted onto the guide wire.
    • 一种单独的可输送栓塞保护装置过滤器,其连接到常规引导件的远端处的螺旋线圈,用于血管中,当进行介入手术以捕获可能产生并释放到血流中的任何栓塞物质时 步骤。 该装置包括具有近端和远端的过滤器组件和连接到过滤器组件的远端的导丝连接器。 导丝连接器能够与导丝的螺旋线圈耦合。 以同轴布置放置在过滤器组件上方的限制护套将过滤器组件保持在折叠位置并将过滤器组件分别输送到导丝的螺旋线圈,然后导丝连接器连接到螺旋线圈。 或者,引导线可以包括可旋转的线圈部分,其形成导丝上的远端尖端线圈的一部分,其适于联接到过滤器组件。 这种布置允许过滤器组件可旋转地安装在导丝上。
    • 58. 发明申请
    • GUIDE WIRE WITH EMBOLIC FILTERING ATTACHMENT
    • 导线与导线连接
    • US20090131971A1
    • 2009-05-21
    • US12025404
    • 2008-02-04
    • Douglas H. GessweinWayne E. CornishScott J. HuterBenjamin C. HuterJohn E. Papp
    • Douglas H. GessweinWayne E. CornishScott J. HuterBenjamin C. HuterJohn E. Papp
    • A61M29/00
    • A61F2/013A61F2002/018A61F2230/0006A61F2230/0067A61F2230/008
    • A separate deliverable embolic protection device filter that attaches to a helical coil at a distal end of a conventional guide, for use in a blood vessel when an interventional procedure is being performed to capture any embolic material which may be created and released into the bloodstream during the procedure. The device includes a filter assembly with a proximal end and a distal end, and a guide wire connector attached to the distal end of the filter assembly. The guide wire connector is able to couple with the helical coil of the guide wire. A restraining sheath placed over the filter assembly in a coaxial arrangement maintains the filter assembly in a collapsed position and delivers the filter assembly separately to the helical coil of the guide wire, and then the guide wire connector is joined to the helical coil. Alternatively, the guide wire can include a rotatable coil section forming a portion of the distal tip coil on the guide wire which is adapted to be coupled to the filter assembly. This arrangement allows the filter assembly to be rotatably mounted onto the guide wire.
    • 一种单独的可输送栓塞保护装置过滤器,其连接到常规引导件的远端处的螺旋线圈,用于血管中,当进行介入手术以捕获可能产生并释放到血流中的任何栓塞物质时 步骤。 该装置包括具有近端和远端的过滤器组件和连接到过滤器组件的远端的导丝连接器。 导丝连接器能够与导丝的螺旋线圈耦合。 以同轴布置放置在过滤器组件上方的限制护套将过滤器组件保持在折叠位置并将过滤器组件分别输送到导丝的螺旋线圈,然后导丝连接器连接到螺旋线圈。 或者,引导线可以包括可旋转的线圈部分,其形成导丝上的远端尖端线圈的一部分,其适于联接到过滤器组件。 这种布置允许过滤器组件可旋转地安装在导丝上。
    • 60. 发明授权
    • Guidewire with an intermediate variable stiffness section
    • 导丝具有中间可变刚度部分
    • US06524301B1
    • 2003-02-25
    • US09748294
    • 2000-12-21
    • W. Stan WilsonRobert C. EsselsteinWayne E. CornishMark T. Richardson
    • W. Stan WilsonRobert C. EsselsteinWayne E. CornishMark T. Richardson
    • A61M2500
    • A61M25/09A61M2025/09083A61M2025/09133
    • The invention is directed to an guide wire for intraluminal deployment of a medical device within a patient, the guide wire having an elongate core member with an intermediate core section comprising a plurality of contiguous segments in alignment with the longitudinal axis of the core member with alternating flexible and rigid core segments, so that the articulated section bends in a discontinuous, discrete manner when advanced through a curved blood vessel or other body lumen within the patient. When an obstruction on a vessel wall causes the catheter or other coaxial device to be impeded, the guide wire and intermediate core section may alternately be advanced and retracted a short distance through the catheter distal tip causing a “nodding” motion of the catheter tip while the catheter is pushed through the vessel, so as to avoid and bypass the vessel obstruction.
    • 本发明涉及一种用于在患者体内腔内部署医疗装置的导丝,所述导丝具有细长的芯部件,所述细长的芯部件具有中间的芯部分,所述中间纤芯部分包括与所述芯部件的纵向轴线对准的多个连续部分, 柔性和刚性的芯段,使得铰接部分在通过患者体内的弯曲血管或其他体腔前进时以不连续的离散方式弯曲。 当血管壁上的阻塞物导致导管或其它同轴装置被阻碍时,引导线和中间芯部分可以交替地前进并缩回穿过导管远端的短距离,导致导管末端的“点头”运动,同时 导管被推过血管,以避免和绕过血管阻塞。