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    • 1. 发明授权
    • Prosthetic heart valves
    • 假心脏瓣膜
    • US09572660B2
    • 2017-02-21
    • US12451678
    • 2008-06-04
    • Peter N. BraidoYousef F. Alkhatib
    • Peter N. BraidoYousef F. Alkhatib
    • A61F2/82A61F2/24A61L27/36A61L27/54
    • A61F2/2418A61F2210/0076A61F2220/0016A61F2220/0075A61F2230/0054A61F2230/008A61L27/3604A61L27/54
    • A prosthetic heart valve (10) (e.g., a prosthetic aortic valve) is designed to be somewhat circumferentially collapsible and then re-expandable. The collapsed condition may be used for less invasive delivery of the valve into a patient. When the valve reaches the implant site in the patient, it re-expands to normal operating size, and also to engage surrounding tissue of the patient. The valve includes a stent portion (200) and a ring portion (100) that is substantially concentric with the stent portion but downstream from the stent portion in the direction of blood flow through the implanted valve. When the valve is implanted, the stent portion engages the patient's tissue at or near the native valve annulus, while the ring portion engages tissue downstream from the native valve site (e.g., the aorta).
    • 假体心脏瓣膜(10)(例如,假体主动脉瓣)被设计成有些周向可折叠并且然后再膨胀。 折叠状态可以用于将瓣膜侵入性较差的患者。 当阀门到达病人的植入部位时,它会重新扩大到正常的操作大小,并且还可以接合病人的周围组织。 所述阀包括支架部分(200)和环状部分(100),所述支架部分(100)与所述支架部分基本上同心,但在所述支架部分的下游沿着通过所述植入瓣膜的血流方向。 当植入瓣膜时,支架部分在天然瓣膜环处或附近接合患者组织,而环部分接合自然瓣膜部位(例如,主动脉)下游的组织。
    • 2. 发明申请
    • PROSTHETIC HEART VALVES
    • 先天性心脏瓣膜
    • US20100168839A1
    • 2010-07-01
    • US12451678
    • 2008-06-04
    • Peter N. BraidoYousef F. Alkhatib
    • Peter N. BraidoYousef F. Alkhatib
    • A61F2/82A61F2/24
    • A61F2/2418A61F2210/0076A61F2220/0016A61F2220/0075A61F2230/0054A61F2230/008A61L27/3604A61L27/54
    • A prosthetic heart valve (10) (e.g., a prosthetic aortic valve) is designed to be somewhat circumferentially collapsible and then re-expandable. The collapsed condition may be used for less invasive delivery of the valve into a patient. When the valve reaches the implant site in the patient, it re-expands to normal operating size, and also to engage surrounding tissue of the patient. The valve includes a stent portion (200) and a ring portion (100) that is substantially concentric with the stent portion but downstream from the stent portion in the direction of blood flow through the implanted valve. When the valve is implanted, the stent portion engages the patient's tissue at or near the native valve annulus, while the ring portion engages tissue downstream from the native valve site (e.g., the aorta).
    • 假体心脏瓣膜(10)(例如,假体主动脉瓣)被设计成有些周向可折叠并且然后再膨胀。 折叠状态可以用于将瓣膜侵入性较差的患者。 当阀门到达病人的植入部位时,它会重新扩大到正常的操作大小,并且还可以接合病人的周围组织。 所述阀包括支架部分(200)和环状部分(100),所述支架部分(100)与所述支架部分基本上同心,但在所述支架部分的下游沿着通过所述植入瓣膜的血流方向。 当植入瓣膜时,支架部分在天然瓣膜环处或附近接合患者组织,而环部分接合自然瓣膜部位(例如,主动脉)下游的组织。
    • 10. 发明授权
    • Prosthetic aortic heart valves
    • 假体主动脉瓣膜
    • US08728154B2
    • 2014-05-20
    • US12733344
    • 2008-08-21
    • Yousef F. Alkhatib
    • Yousef F. Alkhatib
    • A61F2/24A61F2/06
    • A61F2/2418A61F2/2409A61F2/2445A61F2220/0016A61F2220/0075A61F2230/0054A61F2230/0076
    • A prosthetic aortic valve includes an annular, annulus inflow portion that is designed to reside in or near the patient's native aortic valve annulus, and an annular, aortic outflow portion that is designed to reside in the patient's aorta downstream from at least a portion of the valsalva sinus. The annulus inflow portion and the aortic outflow portion are connected to one another by a plurality of connecting struts that are confined to regions near the commissures of the patient's native aortic valve. The connecting struts are designed to bulge out into the valsalva sinus to help anchor the prosthetic valve in place. The valve is circumferentially collapsible to a relatively small diameter for less-invasive delivery into the patient. The valve circumferentially expands to a larger operational diameter when deployed at the implant site.
    • 假体主动脉瓣包括环形环形流入部分,其被设计为驻留在患者的天然主动脉瓣膜环内或附近,以及环形主动脉流出部分,其被设计为驻留在患者主动脉中的至少一部分 valsalva窦。 环形流入部分和主动脉流出部分通过多个连接支柱彼此连接,所述多个连接支柱被限制在靠近病人天然主动脉瓣的连合处的区域。 连接支柱被设计成凸出到瓦尔萨瓦窦中,以帮助将假肢瓣锚定到位。 瓣膜周向可折叠到相对较小的直径,用于较少侵入性地输送到患者体内。 当部署在植入部位时,阀周向地膨胀到更大的操作直径。