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    • 22. 发明授权
    • Lead system for use with an atrial defibrillator and method
    • 用于心房除颤器的铅系统和方法
    • US5350404A
    • 1994-09-27
    • US130308
    • 1993-10-01
    • John M. AdamsClifton A. AlfernessPaul E. Kreyenhagen
    • John M. AdamsClifton A. AlfernessPaul E. Kreyenhagen
    • A61N1/05A61N1/372A61N1/39
    • A61N1/3918A61N1/056A61N1/0563A61N1/3956A61N1/3962A61N1/395A61N1/3987A61N2001/0585
    • An implantable atrial defibrillator provides a pulse of defibrillating electrical energy to the atria of the heart in synchronism with sensed R waves in response to non-coincident sensing of an R wave at first and second areas of the heart. The defibrillating pulse is provided after a predetermined number of consecutive R waves are non-coincidently sensed to assure reliable synchronization. The atrial defibrillator is also operational in a marker mode wherein a number of synchronization marker pulses are delivered to the heart for detection on an externally generated electrocardiogram. The atrial fibrillation detector of the defibrillator is normally disabled and is activated when the sensed ventricular activity indicates a probability of atrial fibrillation to conserve a depletable power source. A plurality of lead systems are also described for use with the atrial defibrillator which reduce the quantity of electrical energy required to defibrillate the heart and ensure that the delivered atrial defibrillating electrical energy is substantially confined to the atria of the heart.
    • 可植入心房除颤器响应于在心脏的第一和第二区域处的R波的不一致的感测,与感测到的R波同步地向心脏的心房提供除颤电脉冲。 在不一致地感测到预定数量的连续R波之后提供除颤脉冲,以确保可靠的同步。 心房除颤器还可以在标记模式中操作,其中多个同步标记脉冲被传送到心脏以便在外部产生的心电图上进行检测。 除颤器的心房颤动检测器通常被禁用,并且当感测到的心室活动指示心房颤动的概率以节省可消耗的电源时被激活。 还描述了与心房除颤器一起使用的多个引导系统,其减少了除颤心脏所需的电能的量,并确保输送的心房除颤电能基本上限于心脏的心房。
    • 25. 发明申请
    • MANUAL BASAL BOLUS DRUG DELIVERY DEVICE
    • 手动基本的BOLUS药物递送装置
    • US20120215175A1
    • 2012-08-23
    • US13360485
    • 2012-01-27
    • Clifton A. AlfernessJohn M. Adams
    • Clifton A. AlfernessJohn M. Adams
    • A61M5/142
    • A61M5/1424A61M5/1454A61M2005/1405
    • A fully manually powered infusion device provides both basal and bolus delivery of a liquid medicament to a patient. In some embodiments, the device includes a main reservoir that supplies the liquid medicament, an outlet port that delivers the liquid medicament to the patient, a basal dispenser that delivers a substantially constant flow of the liquid medicament to the outlet port, and a manually actuated bolus pump that delivers a bolus dose of the liquid medicament from the main reservoir to the outlet when actuated. The basal medicament supply delivers a volume of the liquid medicament from the main reservoir to the basal dispenser consonant with each actuation of the bolus pump.
    • 完全手动输液装置提供液体药物到患者的基础和推注。 在一些实施例中,该装置包括供给液体药物的主储存器,将液体药物输送给患者的出口端口,将液体药物的基本上恒定的流量输送到出口的基础分配器,以及手动致动 推动泵,其在致动时将液体药物从主容器输送到出口。 基础药物供应器通过每次推动推注泵将一定体积的液体药物从主储存器输送到基础分配器辅助器。
    • 28. 发明授权
    • Disposable infusion device facilitating tissue fold formation for cannula deployment and method
    • 一次性输液装置促进组织折叠形成用于插管部署和方法
    • US07713258B2
    • 2010-05-11
    • US12205655
    • 2008-09-05
    • John M. AdamsClifton A. Alferness
    • John M. AdamsClifton A. Alferness
    • A61M31/00
    • A61M5/14248A61M5/425A61M2005/1405A61M2005/1585
    • A device and method facilitates the forming of a skin fold during deployment of a cannula. The device may be a disposable infusion device and the method comprises adhering, to a skin surface, a base member having a port for receiving a cannula, forming a skin fold having skin surfaces sloping away from opposite sides of the base member, driving a cannula through the port of the base member while maintaining the skin fold, and releasing the skin fold. To facilitate the forming of the skin fold, the device comprises a base having a base surface and a flexible layer member. The flexible layer member has a first surface adjacent the base surface and a second surface adapted to be adhered to a patient's skin. The first surface has a first portion adhered to a portion of the base surface and a second portion adherable to the base surface.
    • 装置和方法有助于在插管期间形成皮肤褶皱。 该装置可以是一次性输注装置,并且该方法包括将具有用于接收套管的端口的基部构件粘附到皮肤表面,形成具有从基部构件的相对侧倾斜的皮肤表面的皮肤褶皱,驱动套管 通过基底构件的端口,同时保持皮肤折叠,并释放皮肤褶皱。 为了促进皮肤褶皱的形成,该装置包括具有基底表面和柔性层部件的基部。 柔性层构件具有邻近基底表面的第一表面和适于粘附到患者皮肤的第二表面。 第一表面具有粘附到基部表面的一部分的第一部分和可粘附到基底表面的第二部分。
    • 30. 发明授权
    • Mitral valve therapy device, system and method
    • 二尖瓣治疗装置,系统及方法
    • US06800090B2
    • 2004-10-05
    • US09855945
    • 2001-05-14
    • Clifton A. AlfernessJohn M. AdamsJohn Melmoth Power
    • Clifton A. AlfernessJohn M. AdamsJohn Melmoth Power
    • A61F206
    • A61F2/2451Y10S623/904
    • An assembly and method for effecting the condition of a mitral valve annulus of a heart includes a guide wire configured to be fed into the coronary sinus of the heart, and a mitral valve annulus therapy device configured to be slidingly received on the guide wire and advanced into the coronary sinus of the heart on the guide wire. A guide tube may further be employed for guiding the device into the coronary sinus. An introducer which may be employed for pushing the device into or pulling device out of the heart has a mechanism for releasably locking to the device. This enables substitution of the device if needed. Also, the crossover point of the circumflex artery and coronary sinus may be determined and avoided when the device is deployed.
    • 用于实现心脏二尖瓣环的状态的组件和方法包括:构造成供给到心脏的冠状窦内的导线,以及构造成滑动地容纳在导丝上并提前的二尖瓣环空间治疗装置 进入导丝的心脏冠状窦。 还可以使用导管来将装置引导到冠状窦中。 可以用于将装置推入或拉出装置离开心脏的导引器具有用于可释放地锁定到装置的机构。 如果需要,这可以替代设备。 此外,当部署装置时,可以确定并避免回旋动脉和冠状窦的交叉点。