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    INTRODUCER ASSEMBLY AND PROTECTIVE SLEEVE THEREFOR
    21.
    发明申请
    INTRODUCER ASSEMBLY AND PROTECTIVE SLEEVE THEREFOR 有权
    介绍组装及其保护套管

    公开(公告)号：US20150290426A1

    公开(公告)日：2015-10-15

    申请号：US14676416

    申请日：2015-04-01

    Applicant: COOK MEDICAL TECHNOLOGIES LLC

    Inventor： Erik E. Rasmussen

    IPC: A61M25/00

    CPC classification number: A61M25/0045 ,  A61F2/962 ,  A61F2210/0004 ,  A61M25/005 ,  A61M25/0053 ,  A61M2025/0004 ,  A61M2025/0042 ,  A61M2025/0046 ,  A61M2025/0681

    Abstract: An introducer assembly includes an introducer element (80), which may have a catheter or sheath (82), a pusher element (84) holding an implantable medical device (88) and a dilator tip (90). The assembly also includes a protective sleeve (72) within which the introducer element (80) is disposed. The protective sleeve (72) is made of an absorbable hydrophilic material which is deployed in a wetted condition and acts as a cushion or barrier between the introducer element (80) and the vessel wall (60). The sleeve can prevent trauma to the vessel during the deployment of the introducer element (80) and as a result can avoid vessel spasm which can occur in delicate vessels such as the cerebral vessels. The introducer assembly may be used for cerebral applications.

    Abstract translation: 导引器组件包括导引器元件（80），其可以具有导管或护套（82），保持可植入医疗装置（88）和扩张器尖端（90）的推动元件（84）。 组件还包括保护套筒（72），导引器元件（80）设置在保护套筒内。 保护套筒（72）由可吸收的亲水材料制成，该亲水材料在润湿状态下展开并且用作导引器元件（80）和容器壁（60）之间的缓冲垫或阻挡层。 套管可以在引导器元件（80）的展开期间防止对容器的创伤，并且因此能够避免容易发生在诸如脑血管的微细血管中的血管痉挛。 导引器组件可用于脑应用。

    Aortic graft device
    23.
    发明授权
    Aortic graft device 有权

    公开(公告)号：US10765505B2

    公开(公告)日：2020-09-08

    申请号：US16258860

    申请日：2019-01-28

    Applicant: Cook Medical Technologies LLC

    Inventor： Erik E. Rasmussen ,  Frank K. Christiansen

    IPC: A61F2/07 ,  A61F2/89 ,  A61F2/06 ,  A61F2/82

    Abstract: An aortic arch device that is a unitary tube of graft material having a crimped unstented portion and a stented portion, a collar at the junction of the crimped unstented portion and the stented portion, at least one fenestration or lateral opening in the graft material to accommodate arteries in the aortic arch. Branches may extend from the fenestrations.

    INTRODUCER FOR DEPLOYING A STENT GRAFT IN A CURVED LUMEN AND STENT GRAFT THEREFOR
    26.
    发明申请
    INTRODUCER FOR DEPLOYING A STENT GRAFT IN A CURVED LUMEN AND STENT GRAFT THEREFOR 审中-公开

    公开(公告)号：US20180110610A1

    公开(公告)日：2018-04-26

    申请号：US15839115

    申请日：2017-12-12

    Applicant: Cook Medical Technologies LLC

    Inventor： Tilo Kölbel ,  Erik E. Rasmussen ,  Bent Oehlenschlaeger ,  Kim Moegelvang Jensen

    IPC: A61F2/07 ,  A61F2/95 ,  A61F2/89

    Abstract: A stent graft for deployment in a curved lumen such as the aortic or thoracic arch comprises a constraining mechanism at its proximal end. A stent provided at the proximal end of the stent graft includes loops of material that co-operate with restraining wires that extend between a central guide wire carrier and a restraining wire cannula. The constraining mechanism acts to maintain the proximal stent constrained at both the proximal and distal ends of the proximal stent. The proximal stent is thus allowed to expand after expansion of the remainder of the stent graft during deployment. In an embodiment, the constraining mechanism acts to constrain two adjacent struts of the proximal stent at three points radially therearound, at the proximal end of the stent and at the distal end of the stent. The proximal stent may then overlap with the interior of an adjacent stent at an inner part of a curved vessel.

    Occlusion balloon
    29.
    发明授权
    Occlusion balloon 有权
    闭塞气球

    公开(公告)号：US09468443B2

    公开(公告)日：2016-10-18

    申请号：US14134341

    申请日：2013-12-19

    Applicant: COOK MEDICAL TECHNOLOGIES LLC

    Inventor： Per Elgaard ,  Erik E. Rasmussen ,  Edwin E. Macatangay ,  Sarah Reeves

    IPC: A61M29/00 ,  A61B17/12

    CPC classification number: A61B17/12136 ,  A61B17/12109 ,  A61B2017/12095

    Abstract: A delivery system for an occlusion balloon includes a delivery catheter and a balloon releasably detached thereto. The balloon can include a base portion that is threaded onto the end of the delivery catheter. The balloon can include a one-way valve or septum in the base portion, through which a filling needle is inserted into a cavity of the balloon. The balloon can be filled with a fluid to expand the balloon and fix the balloon within the patient's body. The balloon can be filled with a hardening material to assist in fixing the balloon in place and occluding the blood vessel. The balloon can include anchoring structure on its outer surface to assist in the fixing the location of the balloon. The delivery device and needle can be detached and withdrawn from the balloon, allowing the septum to close and seal the balloon, leaving the balloon fixed within the body vessel.

    Abstract translation: 用于闭塞气囊的递送系统包括递送导管和可释放地分离到其上的气囊。 气囊可以包括螺纹连接到输送导管的端部上的基部。 气囊可以在基部中包括单向阀或隔膜，通过该单向阀或隔膜将填充针插入气囊的空腔中。 气囊可以充满流体以膨胀气囊并将气囊固定在患者体内。 气球可以填充硬化材料，以帮助将气囊固定在适当位置并阻塞血管。 气囊可以在其外表面上包括锚定结构，以帮助固定气囊的位置。 输送装置和针可以从气囊中分离和取出，允许隔膜闭合并密封气囊，使气囊固定在体内容器内。

    IMPLANT RELEASE MECHANISM
    30.
    发明申请
    IMPLANT RELEASE MECHANISM 有权
    植物释放机制

    公开(公告)号：US20160175129A1

    公开(公告)日：2016-06-23

    申请号：US15055127

    申请日：2016-02-26

    Applicant: COOK MEDICAL TECHNOLOGIES LLC

    Inventor： Erik E. Rasmussen ,  Bent Ohlenschlaeger

    IPC: A61F2/95 ,  A61F2/89 ,  A61F2/844

    CPC classification number: A61F2/95 ,  A61B2017/12054 ,  A61F2/01 ,  A61F2/07 ,  A61F2/844 ,  A61F2/89 ,  A61F2002/9505 ,  A61F2002/9511 ,  A61F2002/9665

    Abstract: An implant release mechanism for releasing, for example, a stent (60) is provided with three restraining wires (62) which pass in the space between a wire guide catheter (24) and a pusher sheath or dilator (30) and are arranged substantially equi-angularly threrearound. Each restraining wire (62) holds both the proximal and distal ends of the stent (60), in this case each holding a proportion of the ends of the stent (60). When the restraining wires (62) are pulled they will first unwrap from the proximal end of the stent (60) and will then release the distal end of the stent (60) so as to allow the stent to become fully deployed within the lumen of the patient. The use of common release wires improves deployment of implants and reduces the number and volume of components in the device, thereby allowing it to occupy a smaller volume.

    Abstract translation: 用于释放例如支架（60）的植入物释放机构设置有三条限制线（62），其限制在导线导管（24）和推动器护套或扩张器（30）之间的空间中，并且基本上布置 平等的三分之一。 每个限制线（62）保持支架（60）的近端和远端，在这种情况下，每个限制线都保持支架（60）的端部的一部分。 当约束线（62）被拉动时，它们将首先从支架（60）的近端展开，然后释放支架（60）的远端，以便使支架完全展开在 患者。 使用常见的释放线可改善植入物的部署，并减少装置中部件的数量和体积，从而使其占据较小的体积。

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