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    • 1. 发明申请
    • EMBOLIC PROTECTION DEVICES
    • 嵌入式保护装置
    • US20070208374A1
    • 2007-09-06
    • US11747459
    • 2007-05-11
    • William BoyleAndy DenisonBenjamin HuterScott HuterRichard StackKent StalkerChristopher TarapataJohn Whitfield
    • William BoyleAndy DenisonBenjamin HuterScott HuterRichard StackKent StalkerChristopher TarapataJohn Whitfield
    • A61F2/01A61M29/00
    • A61F2/013A61F2002/011A61F2002/015A61F2002/018A61F2230/0006A61F2230/0067A61F2230/008
    • An embolic protection device for use in a blood vessel when an interventional procedure is being performed in a stenosed or occluded region to capture any embolic material which may be created and released into the bloodstream during the procedure. The device includes a filtering assembly having a self-expanding strut assembly and a filter element attached thereto. In one embodiment, the filtering assembly is attached to the distal end of a guide wire and is deployed within the patient's vasculature as the guide wire is manipulated into the area of treatment. A restraining sheath placed over the filtering assembly in a coaxial arrangement maintains the filtering assembly in its collapsed position until it is ready to be deployed by the physician. Thereafter, the sheath can be retracted to expose the filtering assembly which will then self-expand within the patient's vasculature. Interventional devices can be delivered over the guide wire and any embolic debris created during the interventional procedure and released into the blood stream will enter the filtering assembly and be captured therein. Other embodiments include filtering assemblies attached to an outer tubular member and inner shaft member which apply axial force to the distal ends of the assembly to either expand or contract the struts as needed.
    • 一种用于血管中的栓塞保护装置,当在狭窄或闭塞区域进行介入手术以捕获可能在手术期间产生和释放到血流中的任何栓塞物质。 该装置包括具有自扩张支柱组件和附接到其上的过滤元件的过滤组件。 在一个实施例中,过滤组件附接到导丝的远端,并且当导丝被操纵进入治疗区域时,其被布置在患者的脉管系统内。 以同轴布置放置在过滤组件上方的限制护套将过滤组件保持在其收缩位置,直到其准备好由医师部署。 此后,护套可缩回以露出过滤组件,然后过滤组件将在患者的脉管系统内自我扩张。 介入装置可以在导丝上传送,并且在介入手术期间产生的并释放到血流中的任何栓塞碎片将进入过滤组件并被捕获在其中。 其他实施例包括附接到外部管状构件和内部轴构件的过滤构件,其向组件的远端施加轴向力,以根据需要来扩展或收缩支柱。
    • 2. 发明申请
    • Embolic protection devices
    • 栓塞保护装置
    • US20070167975A1
    • 2007-07-19
    • US11651667
    • 2007-01-10
    • William BoyleDavid BurkettAndy DenisonBenjamin HuterScott HuterArkady KokishKent StalkerChicheng WangJohn Whitfield
    • William BoyleDavid BurkettAndy DenisonBenjamin HuterScott HuterArkady KokishKent StalkerChicheng WangJohn Whitfield
    • A61M29/00
    • A61F2/013A61F2002/011A61F2002/015A61F2002/018A61F2230/0006A61F2230/005A61F2230/0067A61F2230/008
    • An embolic protection device for use in a blood vessel when an interventional procedure is being performed in a stenosed or occluded region to capture any embolic material which may be created and released into the bloodstream during the procedure. The device includes a filtering assembly having a self-expanding strut assembly and a filter element attached thereto. In one embodiment, the filtering assembly is attached to the distal end of a guidewire and is deployed within the patient's vasculature as the guidewire is manipulated into the area of treatment. A restraining sheath placed over the filtering assembly in a coaxial arrangement maintains the filtering assembly in its collapsed position until it is ready to be deployed by the physician. Thereafter, the sheath can be retracted to expose the filtering assembly which will then self-expand within the patient's vasculature. Interventional devices can be delivered over the guidewire and any embolic debris created during the interventional procedure and released into the blood stream will enter the filtering assembly and be captured therein. Other embodiments include filtering assemblies attached to an outer tubular member and inner shaft member which apply axial force to the distal ends of the assembly to either expand or contract the struts as needed.
    • 一种用于血管中的栓塞保护装置,当在狭窄或闭塞区域进行介入手术以捕获可能在手术期间产生和释放到血流中的任何栓塞物质。 该装置包括具有自扩张支柱组件和附接到其上的过滤元件的过滤组件。 在一个实施例中,过滤组件附接到导丝的远端,并且当导线被操纵进入治疗区域时,其部署在患者的脉管系统内。 以同轴布置放置在过滤组件上方的限制护套将过滤组件保持在其收缩位置,直到其准备好被医师部署为止。 此后,护套可缩回以露出过滤组件,然后过滤组件将在患者的脉管系统内自我扩张。 介入装置可以在导丝上传送,并且在介入手术期间产生的并释放到血流中的任何栓塞碎片将进入过滤组件并被捕获在其中。 其他实施例包括附接到外部管状构件和内部轴构件的过滤构件,其向组件的远端施加轴向力,以根据需要来扩展或收缩支柱。
    • 5. 发明申请
    • EXPANDABLE DEVICES
    • US20140012364A1
    • 2014-01-09
    • US13819846
    • 2011-08-30
    • Andy Edward DenisonKent StalkerMark Bates
    • Andy Edward DenisonKent StalkerMark Bates
    • A61F2/82
    • A61F2/89A61F2/04A61F2/82A61F2/915A61F2002/91525A61F2002/91541A61F2002/91558A61F2230/0054A61F2230/0069
    • An expandable, bistable open cell design incorporates the following features: a first relatively stiff portion (152) having first and second ends and a first relatively flexible portion (154) connected to the first and second ends of the first relatively stiff portion, the first relatively stiff portion and the first relatively flexible portion substantially surrounding a first open area (156) of the stent structure; a second relatively stiff portion (158) having first and second ends and a second relatively flexible portion (160) connected to the first and second ends of the first relatively stiff portion, the first relatively stiff portion and the first relatively flexible portion substantially surrounding a second open area (162) of the stent structure; and an opening (1 10) formed through the first relatively stiff portion and the second relatively flexible portion such that the opening connects the first and second open areas, thereby creating first and second intermediate ends (152a, 152b) of the first relatively stiff portion and first and second intermediate ends (160a, 160b) of the second relatively flexible portion. The first intermediate end (152a) of the relatively stiff portion is connected to the first intermediate end (160a) of the relatively flexible portion so as to create a first inward apex (170), the second intermediate end (152b) of the relatively stiff portion is connected to the second intermediate end (160b) of the relatively flexible portion so as to create a second inward apex (172), and the stent structure is configured such that, in a collapsed configuration, the first inward apex (170) is in contact with the second inward apex (172) and, in an expanded configuration, the first inward apex is biased to move in a first circumferential direction and the second inward apex is biased to move in a second circumferential direction that is different than the first circumferential direction.