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    • 35. 发明申请
    • ULTRASOUND ENDOVASCULAR CLEARING DEVICE
    • 超声内镜清除装置
    • WO2009082634A1
    • 2009-07-02
    • PCT/US2008/086558
    • 2008-12-12
    • ST. JUDE MEDICAL, ATRIAL FIBRILLATION DIVISION, INC.SLIWA, John, W.
    • SLIWA, John, W.
    • A61B17/00
    • A61B17/22012A61B2017/22015A61B2017/22017
    • An ultrasonic endovascular clearing device for use in a bodily lumen includes a powering handle configured to enclose one or more acoustic drivers (14), an acoustic amplifier and/or acoustic matching section including one or more amplifiers and/or matching elements (16) and a driven wire (18). The acoustic drivers (14) are configured to produce acoustic vibration in the ultrasonic frequency range. The amplifier/matching section (16) matches and amplifies the acoustic vibration and drives the wire (18) accordingly. The wire (18) cleans due to one or both of a) its asymmetric shape being driven, b) its feature-enhanced surface being driven, whether on an asymmetric wire or not. The driving is pulsed or continuous, cavitating or noncavitating, and torsional or radial/lateral in its possible operational embodiments. A drug may be used by or delivered by the device and wire/tissue parameter sensing is optionally provided.
    • 用于身体管腔的超声波血管内清除装置包括配置成封闭一个或多个声学驱动器(14)的动力手柄,包括一个或多个放大器和/或匹配元件(16)的声学放大器和/或声学匹配部分,以及 驱动线(18)。 声学驱动器(14)构造成在超声波频率范围内产生声振动。 放大器/匹配部分(16)匹配和放大声振动并相应地驱动线(18)。 线(18)由于a)其不对称形状被驱动中的一个或两个而被清洁,b)其特征增强表面被驱动,无论是否在非对称线上。 在其可能的操作实施例中,驱动是脉冲式或连续的,气蚀的或非驱动的,以及扭转的或径向的/侧向的。 药物可以由装置使用或输送,并且可选地提供线/组织参数感测。
    • 39. 发明申请
    • SELF-LOCKING WIRE LOCK
    • 自锁线锁
    • WO2008083337A2
    • 2008-07-10
    • PCT/US2007/089132
    • 2007-12-28
    • ST. JUDE MEDICAL, ATRIAL FIBRILLATION DIVISION, INC.TEGG, Troy Terrance
    • TEGG, Troy Terrance
    • F16B37/12
    • A61M25/0133A61M25/01A61M2025/09125Y10T24/3969Y10T24/3996
    • A wire lock includes a body having an opening therethrough, a locking member disposed at least partially within the opening, and a biasing device. The biasing device urges the locking member into a configuration wherein a wire passing through the opening is restrained in at least one direction, and may operate in either tension or compression. The locking member may include one or more locking elements that are compressed about the wire through engagement with a wedge-shaped locking section of the body, with the biasing member urging the locking member against the locking section. In other embodiments, the locking member is a locking pin riding on an inclined surface of an elongate slot extending across the body, with the biasing member urging the locking pin against one end of the slot, and the wire pinched between the pin and a body surface opposite the inclined surface.
    • 线锁包括具有穿过其中的开口的主体,至少部分地设置在开口内的锁定构件以及偏置装置。 偏置装置将锁定构件推动成这样的构造,其中穿过开口的线在至少一个方向上被限制,并且可以以拉伸或压缩的方式操作。 锁定构件可以包括一个或多个锁定元件,该锁定元件通过与主体的楔形锁定部分接合而围绕线材压缩,偏置构件将锁定构件推压到锁定部分上。 在其他实施例中,锁定构件是骑跨在延伸穿过主体的细长狭槽的倾斜表面上的锁定销,偏置构件将锁定销推压到狭槽的一端上,并且线材夹在销和主体 表面与斜面相对。
    • 40. 发明申请
    • NAVIGATIONAL REFERENCE DISLODGEMENT DETECTION METHOD AND SYSTEM
    • 导航参考推荐检测方法和系统
    • WO2008083111A1
    • 2008-07-10
    • PCT/US2007/088675
    • 2007-12-21
    • ST. JUDE MEDICAL, ATRIAL FIBRILLATION DIVISION, INC.HAUCK, John A.
    • HAUCK, John A.
    • A61B5/05
    • A61B5/06A61B5/042A61B5/063A61B5/7221A61B34/20A61B2034/2051A61B2034/2053A61B2034/2072
    • A method of tracking a position of a catheter within a patient includes securing a navigational reference at a reference location within the patient, defining the reference location as the origin of a coordinate system, determining a location of an electrode moving within the patient relative to that coordinate system, monitoring for a dislodgement of the navigational reference from the initial reference location, for example by measuring the navigational reference relative to a far field reference outside the patient's body, and generating a signal indicating that the navigational reference has dislodged from the reference location. Upon dislodgement, a user may be provided with guidance to help reposition and secure the navigational reference to the initial reference location, or the navigational reference may be automatically repositioned and secured to the initial reference location. Alternatively, a reference adjustment may be calculated to compensate for the changed reference point/origin.
    • 跟踪患者体内导管位置的方法包括:将导航参考固定在患者体内的参考位置处,将参考位置定义为坐标系的原点,确定 在患者体内相对于该坐标系移动的电极,例如通过测量相对于患者身体外部的远场参考的导航参考,监测从初始参考位置移动导航参考,以及生成指示 导航参考已从参考位置移出。 在移位时,可以向用户提供指导以帮助重新定位并确保对初始参考位置的导航参考,或者可以自动重新定位导航参考并将其固定到初始参考位置。 或者,可以计算参考调整以补偿改变的参考点/原点。