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    Endovascular implant for the injection of an active substance into the media of a blood vessel
    1.
    发明申请
    Endovascular implant for the injection of an active substance into the media of a blood vessel 审中-公开
    用于将活性物质注入血管介质的血管内植入物

    公开(公告)号：US20050027350A1

    公开(公告)日：2005-02-03

    申请号：US10630355

    申请日：2003-07-30

    申请人： Carsten Momma ,  Andreas Becker ,  Robert Schmiedl ,  Bernd Heublein

    发明人： Carsten Momma ,  Andreas Becker ,  Robert Schmiedl ,  Bernd Heublein

    IPC分类号： A61F2/00 ,  A61F2/02 ,  A61F2/06

    CPC分类号： A61F2/06 ,  A61F2/2493 ,  A61F2250/0067 ,  A61F2250/0068

    摘要： The invention concerns an endovascular implant for the application of an active substance into the media 22 of a blood vessel and two processes for the production thereof. A base body 42 of the implant has at least in portion-wise manner at a surface 40 which is towards the blood vessel, a plurality of microdevices 10 for injection of the active substance. Each microdevice 10 includes on the one hand at least one microcannula 38 which is raised out of the surface 40 of the implant to such an extent that, when the implant bears against a wall 12 of the blood vessel in surface contact, the microcannula penetrates into the media 22 of the blood vessel, and on the other hand at least one active substance deposit 36 which is in communication with at least one microcannula 38.

    摘要翻译： 本发明涉及一种用于将活性物质施用到血管的介质22中的血管内植入物和用于其生产的两种方法。 植入物的基体42至少部分地位于朝向血管的表面40上，多个微型装置10用于注射活性物质。 每个微型装置10一方面包括至少一个微型插管38，该微型插管38从植入物的表面40升高到这样的程度，使得当植入物抵靠血管的壁12表面接触时，微型插管穿入 血管的介质22，另一方面存在与至少一个微型插管38连通的至少一个活性物质沉积物36。

    Implantation device
    2.
    发明授权
    Implantation device 有权
    植入装置

    公开(公告)号：US09095435B2

    公开(公告)日：2015-08-04

    申请号：US13364639

    申请日：2012-02-02

    申请人： Alexander Rzany ,  Matthias Fringes ,  Alexander Borck ,  Robert Schmiedl ,  Claus Harder

    发明人： Alexander Rzany ,  Matthias Fringes ,  Alexander Borck ,  Robert Schmiedl ,  Claus Harder

    IPC分类号： A61F2/24

    CPC分类号： A61F2/2427 ,  A61F2/2409 ,  A61F2/2418 ,  A61F2/243 ,  A61F2230/0065 ,  A61F2230/0067 ,  A61F2230/0078 ,  A61F2250/001 ,  A61F2250/006

    摘要： The invention relates to an implantation device (10a-d) comprising at least one medical implant (12a-d) and at least one implantation aid (14a-d) comprising at least one expansion element (16a-d). It is provided that the expansion element (16a-d) can be inserted into at least one cavity (18a-d) of the implant (12a-d), and the at least one cavity (18a-d) can be expanded using the expansion element (16a-d), and, in the end state, the expansion element (16a-d) is disposed at least partially in the at least one cavity (18a-d), wherein the expansion element (16a-d) is designed as a solid body (20a-d).

    摘要翻译： 本发明涉及包括至少一个医疗植入物（12a-d）和至少一个包括至少一个膨胀元件（16a-d）的植入辅助器（14a-d）的植入装置（10a-d）。 提供了膨胀元件（16a-d）可以插入到植入物（12a-d）的至少一个空腔（18a-d）中，并且可以使用 膨胀元件（16a-d），并且在最终状态下，膨胀元件（16a-d）至少部分地设置在至少一个空腔（18a-d）中，其中膨胀元件（16a-d）是 设计为固体（20a-d）。

    IMPLANTATION DEVICE
    3.
    发明申请
    IMPLANTATION DEVICE 有权
    植入装置

    公开(公告)号：US20120203331A1

    公开(公告)日：2012-08-09

    申请号：US13364639

    申请日：2012-02-02

    申请人： Alexander Rzany ,  Matthias Fringes ,  Alexander Borck ,  Robert Schmiedl ,  Claus Harder

    发明人： Alexander Rzany ,  Matthias Fringes ,  Alexander Borck ,  Robert Schmiedl ,  Claus Harder

    IPC分类号： A61F2/24

    CPC分类号： A61F2/2427 ,  A61F2/2409 ,  A61F2/2418 ,  A61F2/243 ,  A61F2230/0065 ,  A61F2230/0067 ,  A61F2230/0078 ,  A61F2250/001 ,  A61F2250/006

    摘要： The invention relates to an implantation device (10a-d) comprising at least one medical implant (12a-d) and at least one implantation aid (14a-d) comprising at least one expansion element (16a-d). It is provided that the expansion element (16a-d) can be inserted into at least one cavity (18a-d) of the implant (12a-d), and the at least one cavity (18a-d) can be expanded using the expansion element (16a-d), and, in the end state, the expansion element (16a-d) is disposed at least partially in the at least one cavity (18a-d), wherein the expansion element (16a-d) is designed as a solid body (20a-d).

    摘要翻译： 本发明涉及包括至少一个医疗植入物（12a-d）和至少一个包括至少一个膨胀元件（16a-d）的植入辅助器（14a-d）的植入装置（10a-d）。 提供了膨胀元件（16a-d）可以插入到植入物（12a-d）的至少一个空腔（18a-d）中，并且可以使用 膨胀元件（16a-d），并且在最终状态下，膨胀元件（16a-d）至少部分地设置在至少一个空腔（18a-d）中，其中膨胀元件（16a-d）是 设计为固体（20a-d）。

    Endoprosthesis
    7.
    发明授权
    Endoprosthesis 有权
    内假体

    公开(公告)号：US08801771B2

    公开(公告)日：2014-08-12

    申请号：US12955829

    申请日：2010-11-29

    申请人： Robert Schmiedl

    发明人： Robert Schmiedl

    IPC分类号： A61F2/86 ,  A61F2/90

    CPC分类号： A61F2/86 ,  A61F2/90 ,  A61F2/91 ,  A61F2220/0016 ,  A61F2220/0075 ,  A61F2250/0012 ,  A61F2250/0018

    摘要： An endoprosthesis, particularly an intraluminal endoprosthesis, having a basic structure that is preferably configured in the shape of a hollow cylinder, preferably configured as a basic lattice. In the expanded state, an inner volume enclosed by the basic structure can be changed by means of the elasticity of the basic structure, where the basic structure can assume a normal state and a state of significant compression, with regard to its compression behavior, for further improvement of the healing progression when using an endoprosthesis according to the invention, where in the state of significant compression, the elasticity of the basic structure is significantly reduced as compared with the elasticity in the normal state. The state of significant compression is characterized by the fact that an inside diameter threshold value of the basic structure is not reached, or that a compression pressure threshold value is exceeded. In this connection, the inside diameter threshold value preferably amounts to about 75% of a nominal inside diameter, or the compression pressure threshold value preferably amounts to about 0.2 bar.

    摘要翻译： 具有基本结构的内置假体，特别是管腔内假体，其优选地构造为中空圆柱体的形状，优选地构造为基本格子。 在膨胀状态下，可以通过基本结构的弹性来改变由基本结构包围的内部容积，其中基本结构可以承受正常状态和显着压缩的状态，关于其压缩行为，用于 当使用根据本发明的内置假体时，进一步改善愈合进展，其中在显着压缩的状态下，与正常状态的弹性相比，基本结构的弹性显着降低。 显着压缩的状态的特征在于，没有达到基本结构的内径阈值或超过压缩压力阈值的事实。 在这方面，内径阈值优选地约为标称内径的约75％，或者压缩压力阈值优选地为约0.2巴。

    ENDOPROSTHESIS
    10.
    发明申请
    ENDOPROSTHESIS 有权

    公开(公告)号：US20110190869A1

    公开(公告)日：2011-08-04

    申请号：US12955829

    申请日：2010-11-29

    申请人： Robert Schmiedl

    发明人： Robert Schmiedl

    IPC分类号： A61F2/82

    CPC分类号： A61F2/86 ,  A61F2/90 ,  A61F2/91 ,  A61F2220/0016 ,  A61F2220/0075 ,  A61F2250/0012 ,  A61F2250/0018

    摘要： An endoprosthesis, particularly an intraluminal endoprosthesis, having a basic structure that is preferably configured in the shape of a hollow cylinder, preferably configured as a basic lattice. In the expanded state, an inner volume enclosed by the basic structure can be changed by means of the elasticity of the basic structure, where the basic structure can assume a normal state and a state of significant compression, with regard to its compression behavior, for further improvement of the healing progression when using an endoprosthesis according to the invention, where in the state of significant compression, the elasticity of the basic structure is significantly reduced as compared with the elasticity in the normal state. The state of significant compression is characterized by the fact that an inside diameter threshold value of the basic structure is not reached, or that a compression pressure threshold value is exceeded. In this connection, the inside diameter threshold value preferably amounts to about 75% of a nominal inside diameter, or the compression pressure threshold value preferably amounts to about 0.2 bar.

    摘要翻译： 具有基本结构的内置假体，特别是管腔内假体，其优选地构造为中空圆柱体的形状，优选地构造为基本格子。 在膨胀状态下，可以通过基本结构的弹性来改变由基本结构包围的内部容积，其中基本结构可以承受正常状态和显着压缩的状态，关于其压缩行为，用于 当使用根据本发明的内置假体时，进一步改善愈合进展，其中在显着压缩的状态下，与正常状态的弹性相比，基本结构的弹性显着降低。 显着压缩的状态的特征在于，没有达到基本结构的内径阈值或超过压缩压力阈值的事实。 在这方面，内径阈值优选地约为标称内径的约75％，或者压缩压力阈值优选地为约0.2巴。