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    • 3. 发明授权
    • Prosthesis coupling device and method
    • 假体耦合装置及方法
    • US08277499B2
    • 2012-10-02
    • US12867101
    • 2009-02-11
    • Frank K. ChristiansenKrasnodar Ivancev
    • Frank K. ChristiansenKrasnodar Ivancev
    • A61F2/06
    • A61F2/07A61F2/064A61F2/89A61F2002/067A61F2002/075A61F2220/0075A61F2250/006A61F2250/0063Y10T29/49826
    • A coupling device (28) is formed of a double tubing (50) of a substantially non-porous membrane material, typically a conventional graft material, that is of inner and outer layers of membrane material (52, 54). The inner and outer layers (52, 54) are coupled by bridging rings (56, 58) which allow the layers (52, 54) to be spaced from one another in use. Attached to the inner and outer layers (52, 54) are first and second stents (60, 62). The stent (60) is located on the inside of the double tubing, while the stent (62) is located on the outside of the double tubing (50). The device (28) can expand in effect to ‘bulge’ and thus to fill the gaps to the vessel wall and to the stent-graft sections (24, 26). The device can provide reliable coupling of stent-grafts in vessels of varying diameter or in vessels inflicted with one or more aneurysms.
    • 联接装置(28)由基本上无孔的膜材料(通常是传统的接枝材料)的双层管(50)形成,其为膜材料(52,54)的内层和外层。 内层和外层(52,54)通过桥接环(56,58)联接,桥环使得层(52,54)在使用中彼此间隔开。 附着在内层和外层(52,54)上的是第一和第二支架(60,62)。 支架(60)位于双管的内侧,而支架(62)位于双管(50)的外侧。 装置(28)可以有效地膨胀以膨胀,从而填充到容器壁和支架移植部分(24,26)的间隙。 该装置可以在不同直径的血管或在一个或多个动脉瘤的血管中提供支架移植物的可靠耦合。
    • 4. 发明申请
    • IMPLANT RELEASE MECHANISM
    • 植物释放机制
    • US20110046611A1
    • 2011-02-24
    • US12936107
    • 2009-04-03
    • Frank K. Christiansen
    • Frank K. Christiansen
    • A61M39/00
    • A61F2/95A61F2002/9534
    • A delivery assembly (10) for an implant (30) includes a release mechanism comprising a locking element (52) and a blocking member (56). The locking element (52) includes a latching pin (14) that engages with an eyelet (54) in the implant (30) to attach the implant (30) to a distal end of an inner catheter (36) of the deployment of the delivery assembly (10). The blocking member (56) prevents premature disengagement of the latching pin (14) from the implant (30). Withdrawal of the blocking member (56) allows disengagement of the latching pin (14) once the implant (30) has been correctly positioned within a patient's vasculature. The locking pin (52) and the blocking member (56) extend along the lumen of the inner catheter (36) from a handle (12) at the proximal end thereof, and are arranged such that a guide wire (34) is also able to extend through the lumen of the inner catheter (36). The locking pin (52) and the blocking member (56) preferably have a crescent-shaped transverse cross section. The release mechanism allows an implant (30) to be retrieved either during deployment of the implant (30) to allow the surgeon to correct any mislocation of the implant (30), or in order to remove a previously deployed temporary implant (30) from a patient.
    • 用于植入物(30)的输送组件(10)包括释放机构,其包括锁定元件(52)和阻挡构件(56)。 锁定元件(52)包括与植入物(30)中的孔眼(54)接合以将植入物(30)附接到内部导管(36)的远端的闭锁销(14) 输送组件(10)。 阻挡构件(56)防止闩锁销(14)从植入物(30)过早分离。 一旦植入物(30)已经被正确地定位在病人的血管系统内,则阻塞构件(56)的抽出允许锁定销(14)脱离。 锁定销(52)和阻挡构件(56)在其近端处从手柄(12)沿着内导管(36)的内腔延伸,并且布置成使得导丝(34)也能够 以延伸穿过内导管(36)的内腔。 锁定销(52)和阻挡构件(56)优选地具有月牙形横截面。 释放机构允许在植入物(30)的展开期间回收植入物(30),以允许外科医生校正植入物(30)的任何错位,或者为了从先前部署的临时植入物(30)移除 病人。
    • 5. 发明授权
    • Implant release mechanism
    • 植入物释放机制
    • US08876854B2
    • 2014-11-04
    • US12936107
    • 2009-04-03
    • Frank K. Christiansen
    • Frank K. Christiansen
    • A61M29/00A61F2/06A61F2/95
    • A61F2/95A61F2002/9534
    • A delivery assembly (10) for an implant (30) includes a release mechanism with a locking element (52) and a blocking member (56). The locking element (52) includes a latching pin (14) that engages with an eyelet (54) in the implant (30) to attach the implant (30) to a distal end of an inner catheter (36). The blocking member (56) prevents premature disengagement of the latching pin (14) from the implant (30). Withdrawal of the blocking member (56) allows disengagement of the latching pin (14). The locking pin (52) and the blocking member (56) extend along the lumen of the inner catheter (36) from a handle (12) such that a guide wire (34) is also able to extend through the lumen of the inner catheter (36). The locking pin (52) and the blocking member (56) preferably have a crescent-shaped transverse cross section. The release mechanism allows retrieval of the implant (30).
    • 用于植入物(30)的输送组件(10)包括具有锁定元件(52)和阻挡构件(56)的释放机构。 锁定元件(52)包括与植入物(30)中的孔眼(54)接合以将植入物(30)附接到内部导管(36)的远端的闭锁销(14)。 阻挡构件(56)防止闩锁销(14)从植入物(30)过早分离。 阻挡构件(56)的抽出允许锁定销(14)脱离。 锁定销(52)和阻挡构件(56)从手柄(12)沿着内导管(36)的内腔延伸,使得导丝(34)也能够延伸通过内导管的内腔 (36)。 锁定销(52)和阻挡构件(56)优选地具有月牙形横截面。 释放机构允许取出植入物(30)。
    • 7. 发明申请
    • Prosthesis Coupling Device and Method
    • 假体耦合装置及方法
    • US20110029059A1
    • 2011-02-03
    • US12867101
    • 2009-02-11
    • Frank K. ChristiansenKrasnodar Ivancev
    • Frank K. ChristiansenKrasnodar Ivancev
    • A61F2/82B23P11/00
    • A61F2/07A61F2/064A61F2/89A61F2002/067A61F2002/075A61F2220/0075A61F2250/006A61F2250/0063Y10T29/49826
    • A coupling device (28) is formed of a double tubing (50) of a substantially non-porous membrane material, typically a conventional graft material, that is of inner and outer layers of membrane material (52, 54). The inner and outer layers (52, 54) are coupled by bridging rings (56, 58) which allow the layers (52, 54) to be spaced from one another in use. Attached to the inner and outer layers (52, 54) are first and second stents (60, 62). The stent (60) is located on the inside of the double tubing, while the stent (62) is located on the outside of the double tubing (50). The device (28) can expand in effect to ‘bulge’ and thus to fill the gaps to the vessel wall and to the stent-graft sections (24, 26). The device can provide reliable coupling of stent-grafts in vessels of varying diameter or in vessels inflicted with one or more aneurysms.
    • 联接装置(28)由基本上无孔的膜材料(通常是传统的接枝材料)的双层管(50)形成,其为膜材料(52,54)的内层和外层。 内层和外层(52,54)通过桥接环(56,58)联接,桥环使得层(52,54)在使用中彼此间隔开。 附着在内层和外层(52,54)上的是第一和第二支架(60,62)。 支架(60)位于双管的内侧,而支架(62)位于双管(50)的外侧。 装置(28)可以有效地膨胀成“凸起”,从而将间隙填充到血管壁和支架移植物部分(24,26)。 该装置可以在不同直径的血管或在一个或多个动脉瘤的血管中提供支架移植物的可靠耦合。