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    • 1. 发明申请
    • Insertion Device for Providing Fine Needle Aspiration and Core Biopsy
    • 用于提供细针抽吸和核心活检的插入装置
    • US20130165815A1
    • 2013-06-27
    • US13336482
    • 2011-12-23
    • Kenneth M. ZinnMark Fisher
    • Kenneth M. ZinnMark Fisher
    • A61B10/02
    • A61B10/0275A61B2010/0208
    • An insertion device for taking samples within a body. The insertion device includes a trigger housing, an outer sheath assembly, a sampling device, and a resilient member. The trigger housing includes an interior channel in which the resilient member is disposed to urge the outer sheath assembly away from a proximal end of the trigger housing. The outer sheath assembly is disposed within the interior channel of the trigger housing. The outer sheath assembly includes a body and an outer sheath attached to a distal end of the body. The sampling device is removably disposed within the outer sheath assembly and the trigger housing. The sampling device may be a removable biopsy needle assembly which is used to cock the insertion device. The removable biopsy needle assembly may be removed from the insertion device and be replaced by a needle assembly for fine needle aspiration.
    • 用于在体内取样的插入装置。 插入装置包括触发器壳体,外护套组件,采样装置和弹性构件。 触发器壳体包括内部通道,弹性构件设置在内部通道中,以推动外护套组件远离触发器壳体的近端。 外护套组件设置在触发器壳体的内部通道内。 外护套组件包括主体和附接到主体的远端的外护套。 采样装置可移除地设置在外护套组件和触发器壳体内。 采样装置可以是用于使插入装置旋转的可移除的活检针组件。 可移除的活检针组件可以从插入装置移除,并由用于细针抽吸的针组件代替。
    • 2. 发明授权
    • Insertion device for providing fine needle aspiration and core biopsy
    • 用于提供细针抽吸和核心活检的插入装置
    • US09445790B2
    • 2016-09-20
    • US13336482
    • 2011-12-23
    • Kenneth M. ZinnMark Fisher
    • Kenneth M. ZinnMark Fisher
    • A61B10/02
    • A61B10/0275A61B2010/0208
    • An insertion device for taking samples within a body. The insertion device includes a trigger housing, an outer sheath assembly, a sampling device, and a resilient member. The trigger housing includes an interior channel in which the resilient member is disposed to urge the outer sheath assembly away from a proximal end of the trigger housing. The outer sheath assembly is disposed within the interior channel of the trigger housing. The outer sheath assembly includes a body and an outer sheath attached to a distal end of the body. The sampling device is removably disposed within the outer sheath assembly and the trigger housing. The sampling device may be a removable biopsy needle assembly which is used to cock the insertion device. The removable biopsy needle assembly may be removed from the insertion device and be replaced by a needle assembly for fine needle aspiration.
    • 用于在体内取样的插入装置。 插入装置包括触发器壳体,外护套组件,采样装置和弹性构件。 触发器壳体包括内部通道,弹性构件设置在内部通道中,以推动外护套组件远离触发器壳体的近端。 外护套组件设置在触发器壳体的内部通道内。 外护套组件包括主体和附接到主体的远端的外护套。 采样装置可移除地设置在外护套组件和触发器壳体内。 采样装置可以是用于使插入装置旋转的可移除的活检针组件。 可移除的活检针组件可以从插入装置移除,并由用于细针抽吸的针组件代替。
    • 4. 发明申请
    • Venous Access Port with Molded and/or Radiopaque Indicia
    • 具有模制和/或不透射线标记的静脉进入端口
    • US20120283560A1
    • 2012-11-08
    • US13549998
    • 2012-07-16
    • Timothy M. SchweikertRaymond R. BizupKevin E. SanfordKenneth M. Zinn
    • Timothy M. SchweikertRaymond R. BizupKevin E. SanfordKenneth M. Zinn
    • A61B6/00
    • A61M39/0208A61M5/007A61M2039/0205A61M2039/0229A61M2039/0238A61M2205/32
    • A venous access port assembly having a housing base, a flange, and a septum. The housing base defines an interior reservoir. The flange includes integrally molded X-ray discernable indicia identifying that the assembly is rated for power injection. The X-ray discernable indicia may extend through a height of the flange from a top surface to a bottom surface of the flange. According to one aspect, the flange may be formed from X-ray discernable material, and the X-ray discernable indicia may be formed from the X-ray discernable material of the flange, or they may be formed by voids in the X-ray discernable material. According to another aspect, the flange may be formed from a radiotransparent or radiolucent material and applied with a radiopaque agent, and the X-ray discernable indicia may be one or more voids in the radiopaque agent or may be portions of the flange applied with the radiopaque agent.
    • 具有壳体基座,凸缘和隔膜的静脉通路口组件。 壳体基座定义了内部容器。 凸缘包括整体模制的X射线识别标记,表明该组件额定功率注入。 X射线识别标记可以延伸穿过凸缘的高度从凸缘的顶表面延伸到底表面。 根据一个方面,凸缘可以由X射线可辨别材料形成,并且X射线可辨别标记可以由凸缘的X射线可辨别材料形成,或者它们可以由X射线中的空隙形成 可辨别的材料。 根据另一方面,凸缘可以由无线电透射材料或射线可透过材料形成并且施加不透射线剂,X射线可辨别标记可以是不透射线剂中的一个或多个空隙,或者可以是凸缘部分 不透射线剂。
    • 6. 发明授权
    • Venous access port with molded and/or radiopaque indicia
    • 具有模制和/或不透射线标记的静脉入口
    • US08852160B2
    • 2014-10-07
    • US13549998
    • 2012-07-16
    • Timothy M. SchweikertRaymond R. BizupKevin E. SanfordKenneth M. Zinn
    • Timothy M. SchweikertRaymond R. BizupKevin E. SanfordKenneth M. Zinn
    • A61M35/00A61K9/22A61M39/02
    • A61M39/0208A61M5/007A61M2039/0205A61M2039/0229A61M2039/0238A61M2205/32
    • A venous access port assembly having a housing base, a flange, and a septum. The housing base defines an interior reservoir. The flange includes integrally molded X-ray discernable indicia identifying that the assembly is rated for power injection. The X-ray discernable indicia may extend through a height of the flange from a top surface to a bottom surface of the flange. According to one aspect, the flange may be formed from X-ray discernable material, and the X-ray discernable indicia may be formed from the X-ray discernable material of the flange, or they may be formed by voids in the X-ray discernable material. According to another aspect, the flange may be formed from a radiotransparent or radiolucent material and applied with a radiopaque agent, and the X-ray discernable indicia may be one or more voids in the radiopaque agent or may be portions of the flange applied with the radiopaque agent.
    • 具有壳体基座,凸缘和隔膜的静脉通路口组件。 壳体基座定义了内部容器。 凸缘包括整体模制的X射线识别标记,表明该组件额定功率注入。 X射线识别标记可以延伸穿过凸缘的高度从凸缘的顶表面延伸到底表面。 根据一个方面,凸缘可以由X射线可辨别材料形成,并且X射线可辨别标记可以由凸缘的X射线可辨别材料形成,或者它们可以由X射线中的空隙形成 可辨别的材料。 根据另一方面,凸缘可以由无线电透射材料或射线可透过材料形成并且施加不透射线剂,X射线可辨别标记可以是不透射线剂中的一个或多个空隙,或者可以是凸缘部分 不透射线剂。