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    Catheter Assembly With User-Assisting Handle
    11.
    发明申请
    Catheter Assembly With User-Assisting Handle 有权
    导管装配与用户协助手柄

    公开(公告)号：US20130103130A1

    公开(公告)日：2013-04-25

    申请号：US13279724

    申请日：2011-10-24

    Applicant: Alexander Arthur Lubinski ,  Eric W. Leopold ,  Gerald Ray Martin

    Inventor： Alexander Arthur Lubinski ,  Eric W. Leopold ,  Gerald Ray Martin

    IPC: A61F2/84

    CPC classification number: A61F2/966 ,  A61F2002/9517 ,  A61F2230/0019 ,  A61F2230/0091 ,  A61F2250/0018

    Abstract: A catheter assembly includes a catheter, including an inner member and a sheath, extending from a handle. The handle includes a housing, a braking assembly, a carriage and a carriage driver. The braking assembly comprises a braking element within the housing interior and a braking element rotator. The carriage comprises at least one carriage braking surface engaging the braking element. The carriage driver, such as a spring, biases the carriage towards the proximal end of the handle. The inner member has a proximal end secured to the housing. The sheath has a proximal end secured to the carriage. Rotating the braking element causes the carriage to move proximally as the carriage braking surface slides along the braking element. This causes the sheath to move proximally relative to the inner member.

    Abstract translation: 导管组件包括从手柄延伸的包括内部构件和护套的导管。 手柄包括壳体，制动组件，滑架和滑架驱动器。 制动组件包括壳体内部的制动元件和制动元件旋转器。 滑架包括与制动元件接合的至少一个滑架制动表面。 诸如弹簧的滑架驱动器将滑架偏向手柄的近端。 内部构件具有固定到壳体的近端。 护套具有固定到托架的近端。 当滑架制动表面沿着制动元件滑动时，转动制动元件使滑架向近侧移动。 这使得护套相对于内部构件向近侧移动。

    Catheter assembly with user-assisting handle
    14.
    发明授权
    Catheter assembly with user-assisting handle 有权
    导尿管组件与用户辅助手柄

    公开(公告)号：US08852258B2

    公开(公告)日：2014-10-07

    申请号：US13279724

    申请日：2011-10-24

    Applicant: Alexander Arthur Lubinski ,  Eric W. Leopold ,  Gerald Ray Martin

    Inventor： Alexander Arthur Lubinski ,  Eric W. Leopold ,  Gerald Ray Martin

    IPC: A61F2/06 ,  A61F2/966 ,  A61F2/95

    CPC classification number: A61F2/966 ,  A61F2002/9517 ,  A61F2230/0019 ,  A61F2230/0091 ,  A61F2250/0018

    Abstract: A catheter assembly includes a catheter, including an inner member and a sheath, extending from a handle. The handle includes a housing, a braking assembly, a carriage and a carriage driver. The braking assembly comprises a braking element within the housing interior and a braking element rotator. The carriage comprises at least one carriage braking surface engaging the braking element. The carriage driver, such as a spring, biases the carriage towards the proximal end of the handle. The inner member has a proximal end secured to the housing. The sheath has a proximal end secured to the carriage. Rotating the braking element causes the carriage to move proximally as the carriage braking surface slides along the braking element. This causes the sheath to move proximally relative to the inner member.

    Abstract translation: 导管组件包括从手柄延伸的包括内部构件和护套的导管。 手柄包括壳体，制动组件，滑架和滑架驱动器。 制动组件包括壳体内部的制动元件和制动元件旋转器。 滑架包括与制动元件接合的至少一个滑架制动表面。 诸如弹簧的滑架驱动器将滑架偏向手柄的近端。 内部构件具有固定到壳体的近端。 护套具有固定到托架的近端。 当滑架制动表面沿着制动元件滑动时，转动制动元件使滑架向近侧移动。 这使得护套相对于内部构件向近侧移动。

    Vascular Prosthesis and Methods of Use
    15.
    发明申请
    Vascular Prosthesis and Methods of Use 审中-公开
    血管假体和使用方法

    公开(公告)号：US20130123899A1

    公开(公告)日：2013-05-16

    申请号：US13733755

    申请日：2013-01-03

    Applicant: Eric W. Leopold ,  Gerald Ray Martin ,  Michael Hogendijk ,  John Peckham

    Inventor： Eric W. Leopold ,  Gerald Ray Martin ,  Michael Hogendijk ,  John Peckham

    IPC: A61F2/95

    CPC classification number: A61F2/95 ,  A61F2/885 ,  A61F2/91 ,  A61F2210/0076 ,  A61F2220/0058

    Abstract: An implantable vascular prosthesis is provided for use in a wide range of applications wherein at least first and second helical sections having alternating directions of rotation are coupled to one another. The alternating helical section includes a first and second helical portions each having a flange and having adjacent ends joined directly to one another to define an apex. Each helical portion has a widened flange portion adjacent to the apex, the widened flange portions extending into a space between the helical portions. The prosthesis is configured to conform to a vessel wall without substantially remodeling the vessel, and permits accurate deployment in a vessel without shifting or foreshortening.

    Abstract translation: 提供可植入血管假体用于广泛的应用，其中具有交替的旋转方向的至少第一和第二螺旋部分彼此联接。 交替的螺旋部分包括第一和第二螺旋部分，每个螺旋部分具有凸缘并且具有彼此直接连接以限定顶点的相邻端部。 每个螺旋部分具有与顶点相邻的加宽的凸缘部分，加宽的凸缘部分延伸到螺旋部分之间的空间。 假体构造成符合血管壁而不会使血管基本上重塑，并允许在血管内准确地展开而不需要移位或缩短。

    DELIVERY SYSTEM AND METHOD FOR BIFURCATED GRAFT
    16.
    发明申请
    DELIVERY SYSTEM AND METHOD FOR BIFURCATED GRAFT 有权
    交付系统和方法

    公开(公告)号：US20090132026A1

    公开(公告)日：2009-05-21

    申请号：US11941434

    申请日：2007-11-16

    Applicant: Gerald Ray Martin ,  James R. Watson ,  Isaac J. Zacharias

    Inventor： Gerald Ray Martin ,  James R. Watson ,  Isaac J. Zacharias

    IPC: A61F2/06

    CPC classification number: A61F2/962 ,  A61F2/954 ,  A61F2002/065 ,  A61F2002/9505 ,  A61F2002/9511 ,  A61F2002/9665

    Abstract: A delivery system and method for delivering a bifurcated intracorporeal device. The delivery system comprises a shaft having a distal section supporting a primary support member positioned to be disposed within at least a primary portion of the bifurcated intracorporeal device and a secondary support member extending within a secondary portion of the bifurcated intracorporeal device. At least one belt is configured to be circumferentially disposed about a portion of the secondary support member so to at least partially constrain the secondary portion of the bifurcated intracorporeal device. A tube defining a lumen is secured relative to the secondary support member. A release member is configured to engage and releasably secure the belt in a constraining configuration. The release member extends through at least a portion of the tube lumen such that the release member is accessible adjacent a proximal end of the tube.

    Abstract translation: 用于输送分叉的体内装置的递送系统和方法。 输送系统包括轴，其具有支撑主要支撑构件的远侧部分，该主要支撑构件定位成设置在分叉的体内装置的至少一个主要部分内;以及辅助支撑构件，其在分叉的体内装置的次级部分内延伸。 至少一个带被配置为围绕第二支撑构件的一部分周向地设置，以便至少部分地约束分叉的体内装置的次级部分。 限定内腔的管相对于次级支撑构件固定。 释放构件构造成将带接合并可释放地固定在限制构造中。 释放构件延伸穿过管腔的至少一部分，使得释放构件邻近管的近端可接近。

    Method of making a kink resistant stent-graft
    18.
    发明授权
    Method of making a kink resistant stent-graft 有权

    公开(公告)号：US06361637B1

    公开(公告)日：2002-03-26

    申请号：US09376931

    申请日：1999-08-13

    Applicant: Gerald Ray Martin ,  Lilip Lau ,  Scott N. Stonebrook ,  Sharon Lam ,  Troy Thornton

    Inventor： Gerald Ray Martin ,  Lilip Lau ,  Scott N. Stonebrook ,  Sharon Lam ,  Troy Thornton

    IPC: A61F206

    Abstract: A stent-graft including a stent member having an inner surface and an outer surface, a generally tubular graft member and a coupling member that couples the stent member to the graft member. The coupling member, which is the preferred embodiment is in the form of a ribbon, covers only a portion of the inner or outer surface of the stent member and secures the stent member and graft member to one another. Alternatively, the coupling member can be to described as interconnecting less than entirely the inner or outer surface of the graft member to the stent member. With this construction, regions of the stent member do not interfere with the coupling member. Shear stresses between the stent member and the coupling member and the risk of tearing the graft or coupling member or delamination therebetween may be reduced as compared to a fully enveloped stent member. This construction also provides improved flexibility and kink resistance.

    Inflatable implant
    19.
    发明授权
    Inflatable implant 有权

    公开(公告)号：US10201350B2

    公开(公告)日：2019-02-12

    申请号：US12628623

    申请日：2009-12-01

    Applicant: W. Patrick Stephens ,  Gerald Ray Martin

    Inventor： W. Patrick Stephens ,  Gerald Ray Martin

    IPC: A61M29/00 ,  A61B17/12

    Abstract: Described is an inflatable implant suitable for placement in the human body and left there for an indeterminate and potentially lengthy period of time. The implant is one that has a low profile when introduced into the body and a larger profile when it is inflated with one or more filler materials. Depending upon design and use choices the delivered implant may be removable and adjustable in situ in size, position, location, form, and rigidity. Indeed, in some variations, the design of the implant may be such that it may be removed at a potentially fairly lengthy time after implantation. The implant includes at least one bladder wall that generally is at least partially non-elastic (or unexpandable) after the preselected size is reached. The bladder wall will define at least one fillable volume and may form more than one independent fillable volumes. The bladder wall, in some variations, may be partially elastic or expandable to permit adjustment of implant size or configuration after or during delivery. The implant may be used as a supporting structure in a variety of differing body tissues and structures, e.g., in the spine or as a prosthetic in plastic surgery. The implant may also be used in conjunction with other components (often having a springed bias) as a source of movement in controlling the opening of a lumen or duct, that is to say, as a type of on-off valve or as a controlled flow valve. The implant may be used as an occludant within, or adjacent to, a variety of natural or abnormal anatomical body openings, e.g., vascular and genital lumina, aneurysms, ducts, septal defects, fistulae, esophagus, etc. The wall and filler material may be selected to deliver treatment materials the locale of the implant site or to remove amounts of harmful materials from such a region. The implant may, with an appropriate filler material or bladder wall material, be used in cooperation with an appropriate radio frequency (RF) source to cause the increase of a localized internal temperature and a resulting tissue change such as coagulation, ablation, or the like. Methods of using the implant are also described.

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