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    • 2. 发明授权
    • Method of manufacturing an implantable J-shaped lead
    • 可植入J型引线的制造方法
    • US07558632B1
    • 2009-07-07
    • US11459315
    • 2006-07-21
    • Scott Salys
    • Scott Salys
    • A61N1/05
    • A61N1/056
    • An implantable multi-conductor endocardial lead for a cardiac stimulator includes a tubular lead body of flexible resilient insulative material having a first lumen and a smaller diameter tubular member of similar material having a second lumen is coaxially received in the first lumen. An outer coil conductor is received within an annular cavity between the tubular lead body and the tubular member. An elongated inner coil conductor is received within the second lumen. A tip electrode at the distal end of the lead is coupled to the inner coil conductor and a ring electrode proximally spaced from the tip electrode is coupled to the outer coil conductor. All components except for the outer coil conductor have a normally straight configuration and the outer coil conductor is pre-shaped into a generally circular looped configuration such that, upon assembly, the resulting endocardial lead results in a J-configuration at its distal end.
    • 用于心脏刺激器的可植入多导体心内膜包括具有第一管腔的柔性弹性绝缘材料的管状引线本体和具有第二内腔的类似材料的较小直径管状构件同轴地容纳在第一管腔中。 外部线圈导体容纳在管状引线主体和管状构件之间的环形空腔内。 细长的内部线圈导体被容纳在第二内腔内。 在引线的远端处的尖端电极耦合到内部线圈导体,并且与尖端电极向近侧间隔开的环形电极耦合到外部线圈导体。 除了外部线圈导体之外的所有部件具有通常的直线构造,并且外部线圈导体被预成形为大致圆形的环形构造,使得在组装时,所得到的心内膜导线在其远端处导致J形结构。
    • 5. 发明申请
    • BRAIDED IMPLANTABLE MEDICAL LEAD AND METHOD OF MAKING SAME
    • 可植入式医用引线及其制造方法
    • US20110218602A1
    • 2011-09-08
    • US12716519
    • 2010-03-03
    • Greg KampaDorab N. SethnaScott SalysKeith Victorine
    • Greg KampaDorab N. SethnaScott SalysKeith Victorine
    • A61N1/05H01R43/00
    • A61N1/05H01R43/00Y10T29/4921
    • An implantable medical lead disclosed herein may include a longitudinally extending body, a helical anchor and a lead connector end. The longitudinally extending body may include a distal end, a proximal end, a braid-reinforced inner tubular layer extending between the proximal and distal ends, and an outer tubular layer extending between the proximal and distal ends. The braid-reinforced inner tubular layer may extend through the outer tubular layer in a coaxial arrangement. The helical anchor electrode may be operably coupled to a distal end of the braid-reinforced inner tubular layer. The lead connector end may be operably coupled to the proximal end of the body and include a pin contact operably coupled to a proximal end of the braid-reinforced tubular layer. Rotation of the pin contact relative to the lead connector end may cause rotation of the braid-reinforced inner tubular layer within the outer tubular layer, and the resulting rotation of the braid-reinforced inner tubular layer may cause rotation of the helical anchor electrode.
    • 本文公开的可植入医疗引线可以包括纵向延伸体,螺旋锚和引线连接器端。 纵向延伸体可以包括远端,近端,在近端和远端之间延伸的编织增强的内管状层,以及在近端和远端之间延伸的外管层。 编织增强的内部管状层可以以同轴布置延伸穿过外部管状层。 螺旋锚定电极可以可操作地联接到编织物增强的内部管状层的远端。 引导连接器端可以可操作地耦合到主体的近端,并且包括可操作地联接到编织增强管状层的近端的销接触。 销触点相对于引线连接器端部的旋转可能导致编织增强的内部管状层在外部管状层内的旋转,并且编织增强的内部管状层的最终旋转可能导致螺旋锚定电极的旋转。
    • 6. 发明授权
    • Deflectable hollow stylet guidewire system
    • 可偏转中空管心针导丝系统
    • US07890190B1
    • 2011-02-15
    • US11677006
    • 2007-02-20
    • Scott SalysRavi Jain
    • Scott SalysRavi Jain
    • A61N1/00
    • A61N1/056
    • A body implantable lead system includes an over-the-wire lead with a longitudinally extending lumen. A hollow stylet having an outer peripheral surface is introduced into the lumen and an annular resilient blood seal within the lumen may be sealingly positioned between the outer peripheral surface of the stylet and the lead to prevent flow of blood beyond the blood seal and into the lumen in a proximal direction. A guidewire is slidably received within the hollow stylet and includes a tip end which may project through the passage at the distal end of the lead such that relative movement of the guidewire and stylet within the lead is enabled while avoiding friction between the blood seal and the guidewire. Either the guidewire or the stylet may be preshaped for proper placement of the lead for engagement with the body tissue and surrounded by a semi-rigid retractable sheath.
    • 身体可植入引线系统包括具有纵向延伸管腔的线上导线。 具有外周面的中空管心针被引入内腔,并且内腔内的环形弹性血液密封件可以密封地定位在探针的外周表面和引线之间,以防止血液流过血液密封件流入腔内 在近端方向。 引导线可滑动地容纳在中空管心针内,并且包括可以在引线的远端处突出通过通道的尖端,使得导线和探针在引线内的相对运动得以实现,同时避免血液密封和 导丝。 引导线或探针可以被预先成形,以便正确地放置引线以与身体组织接合并且被半刚性的可缩回护套包围。
    • 8. 发明授权
    • Implantable lead and method of making the same
    • 可植入铅及其制作方法
    • US08751018B1
    • 2014-06-10
    • US11855064
    • 2007-09-13
    • Dorab N. SethnaKeith VictorineScott Salys
    • Dorab N. SethnaKeith VictorineScott Salys
    • A61N1/05
    • A61N1/05
    • A method of manufacturing an implantable lead includes providing a core including at least one longitudinal lumen; providing a jacket comprising a reflowable material; positioning the core at least partially within the jacket; and, after positioning, applying heat to cause the material of the jacket to reflow and bond to the core. An implantable lead includes a core including at least one longitudinal lumen; and a jacket comprising a reflowable material. The core may be at least partially disposed within the jacket with the material of the jacket reflow-bonded to the core. The implantable lead may further include at least one lead component associated with at least one of the core and the jacket.
    • 制造可植入引线的方法包括提供包括至少一个纵向内腔的芯; 提供包括可回流材料的护套; 将芯部至少部分地定位在护套内; 并且在定位之后,施加热量以使夹套的材料回流并结合到芯部。 可植入引线包括:芯,其包括至少一个纵向内腔; 以及包括可回流材料的护套。 芯可以至少部分地设置在护套内,套管的材料回流焊接到芯上。 可植入引线还可以包括至少一个与芯和护套中的至少一个相关联的引线部件。
    • 10. 发明授权
    • Implantable stimulation device with isolating system for minimizing magnetic induction
    • 具有隔离系统的植入式刺激装置,用于最小化磁感应
    • US07164950B2
    • 2007-01-16
    • US10285241
    • 2002-10-30
    • Mark W. KrollScott SalysTimothy J. CoxKerwyn Schimke
    • Mark W. KrollScott SalysTimothy J. CoxKerwyn Schimke
    • A61N1/372
    • A61N1/3718A61N1/368
    • An implantable cardiac stimulation device is equipped with an isolation system capable of attenuating or eliminating induction currents flowing through the stimulation device by eliminating induction loops. The isolation system comprises a magnetic insulator configured to shield selected components of the stimulation device from external magnetic fields or radio-frequency (RF) signals. The magnetic insulator comprises a plurality of sensors that are configured to detect the intensity of the external magnetic fields and/or RF signals, and a switch bank that electrically isolates certain components of the stimulation device to eliminate the induction loops. The isolation system further comprises an attenuation system comprised of at least one magnetoresistor disposed along potential induction loops to attenuate induction currents when subjected to undesirable external magnetic fields and/or RF signals.
    • 可植入心脏刺激装置配备有能够通过消除感应环来衰减或消除流过刺激装置的感应电流的隔离系统。 隔离系统包括被配置为将刺激装置的选定部件从外部磁场或射频(RF)信号屏蔽的磁性绝缘体。 磁绝缘体包括被配置为检测外部磁场和/或RF信号的强度的多个传感器,以及电隔离刺激装置的某些部件以消除感应环的开关组。 隔离系统还包括衰减系统,该衰减系统包括至少一个沿电势感应环设置的磁电阻,以在受到不期望的外部磁场和/或RF信号时衰减感应电流。