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    • 1. 发明授权
    • Glucose analysis instrument
    • 葡萄糖分析仪
    • US07695677B2
    • 2010-04-13
    • US11424883
    • 2006-06-19
    • Karl WernerPeter StephanRobert Lorenz
    • Karl WernerPeter StephanRobert Lorenz
    • B01L3/00
    • G06F19/3481A61B5/14532G06F19/00G16H40/63Y10T436/12Y10T436/144444
    • Glucose analysis instrument for diabetics, comprising a measuring device for determining glucose concentration values, a displaying device for displaying glucose concentration values, a signaling device for generating a reminder signal, and a control and evaluation device that comprises a processor and a data memory and is used to determine reminder times at which the signaling device is actuated. Event data are stored in the data memory, the event data containing information on events occurring in the life of a user of the glucose analysis instrument and on the time of occurrence of such events. The reminder times are determined by means of a reminder time determination algorithm taking into consideration event data from at least one previous day.
    • 用于糖尿病患者的葡萄糖分析仪,包括用于测定葡萄糖浓度值的测量装置,用于显示葡萄糖浓度值的显示装置,用于产生提醒信号的信号装置,以及包括处理器和数据存储器的控制和评估装置, 用于确定信号装置被致动的提醒时间。 事件数据存储在数据存储器中,事件数据包含关于在葡萄糖分析仪器的使用者的寿命中发生的事件的信息以及发生这种事件的时间。 提醒时间通过考虑来自至少一个前一天的事件数据的提醒时间确定算法来确定。
    • 2. 发明申请
    • GLUCOSE ANALYSIS INSTRUMENT
    • 葡萄糖分析仪
    • US20060286620A1
    • 2006-12-21
    • US11424883
    • 2006-06-19
    • Karl WernerPeter StephanRobert Lorenz
    • Karl WernerPeter StephanRobert Lorenz
    • C12Q1/54C12M3/00
    • G06F19/3481A61B5/14532G06F19/00G16H40/63Y10T436/12Y10T436/144444
    • Glucose analysis instrument for diabetics, comprising a measuring device for determining glucose concentration values, a displaying device for displaying glucose concentration values, a signaling device for generating a reminder signal, and a control and evaluation device that comprises a processor and a data memory and is used to determine reminder times at which the signaling device is actuated. Event data are stored in the data memory, the event data containing information on events occurring in the life of a user of the glucose analysis instrument and on the time of occurrence of such events. The reminder times are determined by means of a reminder time determination algorithm taking into consideration event data from at least one previous day.
    • 用于糖尿病患者的葡萄糖分析仪,包括用于测定葡萄糖浓度值的测量装置,用于显示葡萄糖浓度值的显示装置,用于产生提醒信号的信号装置,以及包括处理器和数据存储器的控制和评估装置, 用于确定信号装置被致动的提醒时间。 事件数据存储在数据存储器中,事件数据包含关于在葡萄糖分析仪器的使用者的寿命中发生的事件的信息以及发生这种事件的时间。 提醒时间通过考虑来自至少一个前一天的事件数据的提醒时间确定算法来确定。
    • 3. 发明授权
    • Medical system and method for operating a medical system
    • 医疗系统和操作医疗系统的方法
    • US09101307B2
    • 2015-08-11
    • US13445607
    • 2012-04-12
    • Detlef ThymRobert Lorenz
    • Detlef ThymRobert Lorenz
    • G06K7/01A61B5/151A61B5/145A61B19/00
    • A61B5/14532A61B90/90A61B90/98A61B2090/0814A61B2560/029A61B2562/0247G06F19/00
    • A medical system and method to operating the medical system is presented. A patient storage element is assigned to a patient comprising identification information identifying the patient. A medical device has a contaminating patient application. A medical device storage element on the medical device comprises use information. A clearing device receives the identification information from the patient storage element and the use information from the medical device storage element and analyzes the use information. If in analyzing the use information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted. If in analyzing the use information it is found that application of the medical device to the patient is not allowed, the identification information is analyzed. If in analyzing the identification information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted.
    • 介绍了医疗系统和操作医疗系统的方法。 患者存储元件被分配给患者,包括识别患者的识别信息。 医疗器械具有污染的患者应用。 医疗装置上的医疗装置存储元件包括使用信息。 清除装置从患者存储元件接收识别信息和来自医疗装置存储元件的使用信息,并分析使用信息。 如果在分析使用信息时发现允许将医疗装置应用于患者,则输出间隙信号。 如果在分析使用信息中发现不允许将医疗装置应用于患者,则分析识别信息。 如果在分析识别信息时发现允许将医疗装置应用于患者,则输出间隙信号。
    • 5. 发明授权
    • Analysis system for the photometric determination of an analyte in a body fluid
    • 用于体液中分析物的光度测定的分析系统
    • US08481329B2
    • 2013-07-09
    • US12606361
    • 2009-10-27
    • Ulrich PorschRobert Lorenz
    • Ulrich PorschRobert Lorenz
    • G01N21/00
    • G01N21/8483Y10T436/11
    • The invention relates to an analysis system for the photometric determination of an analyte in a body fluid, having an analysis device and a test carrier. The test carrier has an evaluation zone in which a photometrically detectable change takes place as the result of a reaction of a sample of the body fluid which contacts the test carrier with a reagent contained in the test carrier. The analysis device comprises an optical emitter for emitting light onto the evaluation zone, an optical receiver for receiving light from the evaluation zone and for generating a measurement signal corresponding to the received light, and a measurement and evaluation device with a measuring unit and an evaluating unit. The measurement signal is amplified and digitalized in the measuring unit. In the evaluating unit, the concentration value is determined from the digitalized measurement signal. In the evaluating unit, a control value of a control parameter is detected at one detection point during the processing after the calculation step. An error in the measurement and evaluation device is recognized if the deviation of the control value from the expected value exceeds a predefined threshold value.
    • 本发明涉及一种用于对具有分析装置和测试载体的体液中的分析物进行光度测定的分析系统。 测试载体具有评估区,其中由于与测试载体接触的体液的样品与测试载体中包含的试剂的反应而发生光度可检测的变化。 分析装置包括用于将光发射到评估区域的光发射器,用于接收来自评估区域的光并用于产生对应于所接收的光的测量信号的光接收器,以及具有测量单元和评估装置的测量和评估装置 单元。 测量信号在测量单元中放大和数字化。 在评估单元中,从数字化测量信号确定浓度值。 在评估单元中,在计算步骤之后的处理期间的一个检测点处检测控制参数的控制值。 如果控制值与期望值的偏差超过预定义的阈值,则识别测量和评估装置中的错误。
    • 6. 发明申请
    • Medical system and method for operating a medical system
    • 医疗系统和操作医疗系统的方法
    • US20120262274A1
    • 2012-10-18
    • US13445607
    • 2012-04-12
    • Detlef ThymRobert Lorenz
    • Detlef ThymRobert Lorenz
    • G06K7/01A61B5/151
    • A61B5/14532A61B90/90A61B90/98A61B2090/0814A61B2560/029A61B2562/0247G06F19/00
    • A medical system and method to operating the medical system is presented. A patient storage element is assigned to a patient comprising identification information identifying the patient. A medical device has a contaminating patient application. A medical device storage element on the medical device comprises use information. A clearing device receives the identification information from the patient storage element and the use information from the medical device storage element and analyzes the use information. If in analyzing the use information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted. If in analyzing the use information it is found that application of the medical device to the patient is not allowed, the identification information is analyzed. If in analyzing the identification information it is found that application of the medical device to the patient is allowed, a clearance signal is outputted.
    • 介绍了医疗系统和操作医疗系统的方法。 患者存储元件被分配给患者,包括识别患者的识别信息。 医疗器械具有污染的患者应用。 医疗装置上的医疗装置存储元件包括使用信息。 清除装置从患者存储元件接收识别信息和来自医疗装置存储元件的使用信息,并分析使用信息。 如果在分析使用信息时发现允许将医疗装置应用于患者,则输出间隙信号。 如果在分析使用信息中发现不允许将医疗装置应用于患者,则分析识别信息。 如果在分析识别信息时发现允许将医疗装置应用于患者,则输出间隙信号。
    • 9. 发明申请
    • ANALYSIS SYSTEM FOR THE PHOTOMETRIC DETERMINATION OF AN ANALYTE IN A BODY FLUID
    • 体液中分析物的光度测定分析系统
    • US20100075433A1
    • 2010-03-25
    • US12606361
    • 2009-10-27
    • Ulrich PorschRobert Lorenz
    • Ulrich PorschRobert Lorenz
    • G01N21/00
    • G01N21/8483Y10T436/11
    • The invention relates to an analysis system for the photometric determination of an analyte in a body fluid, having an analysis device and a test carrier. The test carrier has an evaluation zone in which a photometrically detectable change takes place as the result of a reaction of a sample of the body fluid which contacts the test carrier with a reagent contained in the test carrier. The analysis device comprises an optical emitter for emitting light onto the evaluation zone, an optical receiver for receiving light from the evaluation zone and for generating a measurement signal corresponding to the received light, and a measurement and evaluation device with a measuring unit and an evaluating unit. The measurement signal is amplified and digitalized in the measuring unit. In the evaluating unit, the concentration value is determined from the digitalized measurement signal. In the evaluating unit, a control value of a control parameter is detected at one detection point during the processing after the calculation step. An error in the measurement and evaluation device is recognized if the deviation of the control value from the expected value exceeds a predefined threshold value.
    • 本发明涉及一种用于对具有分析装置和测试载体的体液中的分析物进行光度测定的分析系统。 测试载体具有评估区,其中由于与测试载体接触的体液的样品与测试载体中包含的试剂的反应而发生光度可检测的变化。 分析装置包括用于将光发射到评估区域的光发射器,用于接收来自评估区域的光并用于产生对应于所接收的光的测量信号的光接收器,以及具有测量单元和评估装置的测量和评估装置 单元。 测量信号在测量单元中放大和数字化。 在评估单元中,从数字化测量信号确定浓度值。 在评估单元中,在计算步骤之后的处理期间的一个检测点处检测控制参数的控制值。 如果控制值与期望值的偏差超过预定义的阈值,则识别测量和评估装置中的错误。