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    • 83. 发明申请
    • Left Atrial Appendage Occluder
    • 左心房闭塞者
    • US20140142612A1
    • 2014-05-22
    • US14122794
    • 2012-05-25
    • Anning LiDeyuan Zhang
    • Anning LiDeyuan Zhang
    • A61B17/12
    • A61B17/12122A61B17/12172A61B17/12177A61B2017/00597A61B2017/00606A61B2017/00619A61B2017/00623A61B2017/1205
    • A left atrial appendage occluder (100) comprises an elastic closure disc (11); the left atrial appendage occluder (100) also comprises a supporting structure (111) connecting with the closure disc (11) and being located on one side of the closure disc, with the supporting structure (111) comprising a central end connecting with the closure disc and a plurality of interconnected and bent struts (121), wherein at least one anchoring thorn (131) is set near the end of at least one strut (121) with the anchoring thorn (131) toward the closure disc (11). The left atrial appendage occluder has a stable structure, a good positioning and sealing effect on the cavity wall in the left atrial appendage, and it is easy to position repeatedly; it can also be recycled before separating from a conveyor. When in surgical operation, the left atrial appendage occluder can select the position area based on the actual shape and size of the patient's left atrial appendage, so the surgical risk is lowered.
    • 左心耳封堵器(100)包括弹性闭合盘(11); 左心耳封堵器(100)还包括与闭合盘(11)连接并位于封闭盘的一侧上的支撑结构(111),支撑结构(111)包括与闭合件连接的中心端 盘和多个互连和弯曲的支柱(121),其中至少一个锚定刺(131)设置在至少一个支柱(121)的端部附近,其中锚定刺(131)朝向封闭盘(11)。 左心耳闭塞器具有稳定的结构,对左心耳腔腔的定位和密封效果好,反复放置容易; 它也可以在与输送机分离之前再循环。 在外科手术中,左心耳阻塞者可以根据患者左心耳的实际形状和大小选择位置区域,从而降低手术风险。
    • 87. 发明公开
    • Left Atrial Appendage Occluder
    • US20240074762A1
    • 2024-03-07
    • US18388154
    • 2023-11-08
    • Lifetech Scientific (Shenzhen) Co., Ltd.
    • Anning LiZhuo Chen
    • A61B17/12A61B17/00
    • A61B17/12122A61B17/00A61B17/0057A61B17/12168A61B2017/00597A61B2017/00632
    • A left atrial appendage occluder (200) comprises a sealing part (220), a fixing part (210) disposed at one side of the sealing part (220), and a connection part (230) for connecting the sealing part (220) and the fixing part (210). The radial deformation capacity of the sealing part (220) is greater than the radial deformation capacity of the fixing part (210), and/or, the axial deformation capacity of the sealing part (220) is greater than the axial deformation capacity of the fixing part (210). In the left atrial appendage occluder (200), the radial or axial deformation capacity of the sealing part (220) is configured to be greater than the radial or axial deformation capacity of the fixing part (210), thereby avoiding the situation in which the sealing part (220) is not optimally fitted with the opening of the left atrial appendage (10) when the fixing part (210) is placed inside of the left atrial appendage (10), which in turn enhances the occlusion effect. Additionally, the sealing part (220) has great deformation capacity which reduces the risks of the sealing part (220) causing abrasion to the opening of the left atrial appendage, or even damaging the opening of the left atrial appendage. The fixing part (210) not only avoids the risks, but also fixes the occluder in the left atrial appendage (10) more effectively, and prevents the occluder (200) from being disengaged from the left atrial appendage.
    • 88. 发明授权
    • Coated stent
    • US11890182B2
    • 2024-02-06
    • US17297229
    • 2019-11-22
    • Shenzhen Lifetech Endovascular Medical Co., Ltd.
    • Benhao XiaoWenjun Pu
    • A61F2/07A61F2/915A61F2/82
    • A61F2/07A61F2/915A61F2002/075A61F2002/825A61F2220/0008A61F2250/0037A61F2250/0039
    • A coated stent (100,200,300,400), comprises a coated unit (110,210,310,410), and an exposed unit (120,220,320,420) which is a ring-shaped structure and which is provided on the periphery (113,213,313) of an end portion (112,212,312) of the coated unit (110,210,310,410); the exposed unit (120,220,320,420) comprises an inward-tilting wave body (122,222,322,422), the inward-tilting wave body (122,222,322,422) comprising at least a first wave crest (122a,222a,322a) and a first wave rod (122c) connected to the first wave crest (122a,222a,322a); the position of the first wave crest (122a.222a,322a) is farther away from the coated unit (110,210,310,410) than other positions on the inward-tilting wave body (122,222,322,422); the first wave rod (122c) is planar, and from the first wave crest (122a,222a,322a) to an end of the exposed unit (120,220,320,420) near the coated unit (110,210,310,410), the radial distance from the inward-tilting wave body (122,222,322,422) to the central axis (102,202,302,402) of the coated unit (110,210,310,410) gradually increases. When the coated stent (100,200,300,400) is implanted into an arterial vessel (10), the inward-tilting wave body (122,222,322,422) forms a certain avoidance space due to the tilt to adapt to the curvature of a large curved side (11) of the arterial vessel (10), and prevents the inward-tilting wave body (122,222,322,422) from directly piercing a branch vessel (20).
    • 89. 发明公开
    • Luminal Stent
    • US20240024137A1
    • 2024-01-25
    • US18268297
    • 2021-11-11
    • Lifetech Scientific (Shenzhen) Co. Ltd.
    • Chunwei Tang
    • A61F2/91A61F2/06A61F2/966
    • A61F2/91A61F2/06A61F2/966A61F2002/9665
    • A luminal stent (100) is provided, including a tubular main body (11) and a semi-releasing device (20) connected to the tubular main body (11). The tubular main body (11) includes a binding area (112) and a non-binding area (111) distributed in a circumferential direction. The semi-releasing device (20) includes a limiting rod (21) located outside the tubular main body (11), and binding lines (22) and limiting fasteners (23) arranged on the tubular main body (11). The binding lines (22) are arranged in the binding area (112). The binding lines (22) each include a fixed end (22a), a binding portion (22b) and a locking portion (22c) which are connected to one another. The fixed ends (22a) are fixedly connected to the tubular main body (11). Both the locking portions (22c) and the limiting fasteners (23) are detachably connected to the limiting rod (21). When both the locking portions (22c) and the limiting fasteners (23) are connected to the limiting rod (21), the binding lines (22) circumferentially constrain the binding area (112). By uniformly compressing a part of a circumferential area of the luminal stent (100), the luminal stent (100) can be in a semi-released state, thereby adjusting and positioning the luminal stent (100), and improving the accuracy of the axial and circumferential positioning of the luminal stent (100).