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    • 3. 发明授权
    • Medical device programming safety
    • 医疗器械编程安全
    • US07885712B2
    • 2011-02-08
    • US11940604
    • 2007-11-15
    • Steven M. GoetzDonald R. JohnsonTouby A. DrewAndrew H. HouchinsJeffrey T. KeacherTheodore J. StoneEarle T. Roberts
    • Steven M. GoetzDonald R. JohnsonTouby A. DrewAndrew H. HouchinsJeffrey T. KeacherTheodore J. StoneEarle T. Roberts
    • A61N1/08
    • G06F19/3481G06F19/00G06F19/3418
    • Techniques for increasing the safety of medical device programming using general purpose hardware, such as a general purpose personal computer, are described. In some embodiments, a system includes an intermediate computing device comprising an applications module. Information from the applications module, such as instructions for an implantable medical device (IMD), may be presented to a user via a user input terminal that is separate from the intermediate computing device. A user may interact with the user input terminal to select an instruction from the applications module, and the intermediate computing device may transmit the selected instruction to the IMD. In some embodiments, the intermediate computing device comprises a web server and the user input terminal comprises a web browser configured to access the web server. In other embodiments, the intermediate computing device comprises a client server and the user input terminal comprises a client.
    • 描述用于增加使用通用硬件(例如通用个人计算机)的医疗设备编程安全性的技术。 在一些实施例中,系统包括包括应用模块的中间计算设备。 可以经由与中间计算设备分离的用户输入终端向用户呈现来自应用模块的信息,诸如可植入医疗设备(IMD)的指令。 用户可以与用户输入终端交互以从应用模块选择指令,并且中间计算设备可以将所选择的指令发送到IMD。 在一些实施例中,中间计算设备包括web服务器,并且用户输入终端包括被配置为访问web服务器的web浏览器。 在其他实施例中,中间计算设备包括客户端服务器,并且用户输入终端包括客户端。
    • 4. 发明申请
    • TRACKING OF COMMUNICATION SESSIONS WITH AN IMPLANTABLE MEDICAL DEVICE
    • 用可植入医疗设备跟踪通信会议
    • US20100274322A1
    • 2010-10-28
    • US12428019
    • 2009-04-22
    • Touby A. Drew
    • Touby A. Drew
    • A61N1/08
    • A61N1/37235A61N1/37247G16H40/40
    • Communication sessions between external devices and implantable medical devices are tracked using a session value that is incremented for each new session and that is stored within the implantable medical device. Session logs that are created for each session may include the session value that is obtained for that session. The session value allows available session logs to be considered in the proper sequence and allows for an awareness of missing session logs. The incrementing of the session value may occur at the external device according to one convention, or at the implantable medical device according to another. The session value to be used for a given session may be the value accessed from the implantable medical device according to one convention or may be the session value that results from incrementing the session value that is accessed from the implantable medical device according to another.
    • 在外部设备和可植入医疗设备之间的通信会话使用对于每个新会话递增并存储在可植入医疗设备内的会话值来跟踪。 为每个会话创建的会话日志可能包括为该会话获取的会话值。 会话值允许以适当的顺序考虑可用的会话日志,并允许意识到缺少的会话日志。 会话值的增加可以根据一个惯例在外部设备处发生,或者根据另一个惯例在可植入医疗设备处发生。 用于给定会话的会话值可以是根据一个约定从可植入医疗设备访问的值,或者可以是从根据另一个可植入医疗设备访问的会话值增加导致的会话值。
    • 5. 发明申请
    • Peak Data Retention of Signal Data In An Implantable Medical Device
    • 可植入医疗器械中信号数据的峰值数据保留
    • US20080235469A1
    • 2008-09-25
    • US12037694
    • 2008-02-26
    • Touby A. Drew
    • Touby A. Drew
    • G06F12/08
    • A61B5/02055A61B5/4094A61B5/7232A61N1/08A61N1/3601A61N1/36082
    • Methods and apparatus for storing data records associated with an extreme value are disclosed. Signal data is stored in a first buffer of a set of buffers. If a local extreme value for the first buffer exceeds a global extreme value, signal data is stored in a second buffer of the set of buffers. This process is repeated, wrapping around and overwriting buffers until the signal data in a current buffer does not have a local extreme value that exceeds the global extreme value. When this happens, signal data may be stored in a subsequent buffer and if a local extreme value of the subsequent buffer does not exceed the global extreme value, further signal data may be stored in the subsequent buffer in a circular manner until either an instantaneous extreme value exceeds the global extreme value or the recording period ends. In an embodiment, the extreme value may be a peak value.
    • 公开了存储与极值相关联的数据记录的方法和装置。 信号数据存储在一组缓冲器的第一缓冲器中。 如果第一缓冲区的局部极值超过全局极值,则信号数据被存储在该组缓冲器的第二缓冲器中。 重复此过程,环绕并覆盖缓冲区,直到当前缓冲区中的信号数据不具有超过全局极值的局部极值。 当这种情况发生时,信号数据可以存储在随后的缓冲器中,并且如果后续缓冲器的局部极值不超过全局极限值,则可以以循环方式将另外的信号数据存储在随后的缓冲器中,直到瞬时极限 值超过全局极值或记录周期结束。 在一个实施例中,极值可以是峰值。
    • 6. 发明申请
    • MEDICAL DEVICE PROGRAMMING SAFETY
    • 医疗设备编程安全
    • US20080140161A1
    • 2008-06-12
    • US11940573
    • 2007-11-15
    • Steven M. GoetzDonald R. JohnsonTouby A. DrewAndrew H. HouchinsJeffrey T. KeacherTheodore J. StoneEarle T. Roberts
    • Steven M. GoetzDonald R. JohnsonTouby A. DrewAndrew H. HouchinsJeffrey T. KeacherTheodore J. StoneEarle T. Roberts
    • A61N1/00
    • G06F19/3481G06F19/00G06F19/3418
    • Techniques for increasing the safety of medical device programming using general purpose hardware, such as a general purpose personal computer, are described. Some embodiments include a watchdog module that is serviced by the general purpose hardware, a mediator module that monitors programming instructions from the general purpose hardware, and/or a safe mode input that may be activated by a user. In some embodiments, a system comprises an implantable medical device, an intermediate device, a computing device that communicates with the implantable medical device via the intermediate device. The intermediate device may provide any one or more of the safety measures described above. In some embodiments, the intermediate device is dedicated hardware, and critical programming functions are provided by the intermediate device, rather than the general purpose hardware. In some embodiments, an implantable medical device provides one or more of the above-discussed safety features, rather than a separate intermediate device.
    • 描述用于增加使用通用硬件(例如通用个人计算机)的医疗设备编程安全性的技术。 一些实施例包括由通用硬件服务的看门狗模块,监视来自通用硬件的编程指令的调解器模块和/或可由用户激活的安全模式输入。 在一些实施例中,系统包括可植入医疗装置,中间装置,经由中间装置与可植入医疗装置通信的计算装置。 中间装置可以提供上述任何一种或多种安全措施。 在一些实施例中,中间设备是专用硬件,并且关键编程功能由中间设备而不是通用硬件提供。 在一些实施例中,可植入医疗装置提供一个或多个上述安全特征,而不是单独的中间装置。