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公开(公告)号：US20120178152A1
公开(公告)日：2012-07-12
申请号：US13357930
申请日：2012-01-25
申请人： Christoph Eisenhardt , Martin Haupt
发明人： Christoph Eisenhardt , Martin Haupt
CPC分类号： A61B5/150358 , A61B5/14532 , A61B5/150022 , A61B5/150305 , A61B5/150412 , A61B5/150503 , A61B5/15186 , A61B5/157
摘要： A medical hand-held device is disclosed comprising a test tape unit that can be inserted into a device housing which comprises a test tape provided with a plurality of analytical test elements which can be wound by means of a spool, and a tape drive comprising an electric motor and a gear unit that can be coupled to the test tape unit for winding the test tape forwards in sections, such that the test elements can successively be provided for sample application. The axis of rotation of the electric motor is arranged in a plane extending transversely to the axis of rotation of the spool and that the gear unit has an angle drive to change the direction of the axis.
摘要翻译： 公开了一种医疗手持式装置，其包括测试带单元，该测试带单元可插入设备壳体中，该测试带单元包括测试带，该测试带设置有可通过线轴缠绕的多个分析测试元件，以及磁带驱动器， 电动机和齿轮单元，其可以耦合到测试带单元，用于将测试带向前卷绕，使得测试元件可以连续地提供用于样品应用。 电动机的旋转轴线布置在横向于卷轴旋转轴线的平面中，并且减速器具有角度驱动以改变轴线的方向。
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公开(公告)号：US08517938B2
公开(公告)日：2013-08-27
申请号：US12767579
申请日：2010-04-26
CPC分类号： A61B90/98 , A61B5/0002 , A61B5/14532 , A61B5/150022 , A61B5/150175 , A61B5/150305 , A61B5/150358 , A61B5/150412 , A61B5/150503 , A61B5/150786 , A61B5/150793 , A61B5/15087 , A61B5/15113 , A61B5/15117 , A61B5/15146 , A61B5/15151 , A61B5/15163 , A61B5/157 , A61B90/96 , A61B2017/00482 , A61B2090/0811 , A61B2562/08
摘要： The invention proposes a medical system which comprises a central control unit which is set up to display at least one diagnostic measured value using a display element. The medical system also comprises at least one invasive unit, wherein the invasive unit has at least one invasive consumable. The invasive consumable is set up to invasively intervene in a tissue of a patient. The invasive unit has at least one contactlessly readable electronic identifier for storing at least one piece of information. The central control unit is set up to electronically read the at least one piece of information in the electronic identifier. The central control unit and the invasive unit are functionally independent of one another such that the respective function of the central control unit and of the invasive unit can be performed independently of the presence of the respective other unit.
摘要翻译： 本发明提出了一种医疗系统，其包括中央控制单元，其被设置为使用显示元件显示至少一个诊断测量值。 所述医疗系统还包括至少一个侵入性单元，其中所述侵入性单元具有至少一种侵入性消耗品。 侵入性消耗品设置为侵入性地介入患者的组织。 侵入单元具有至少一个用于存储至少一条信息的非接触式可读电子标识符。 中央控制单元设置为电子地读取电子标识符中的至少一条信息。 中央控制单元和侵入单元在功能上彼此独立，使得中央控制单元和侵入单元的相应功能可以独立于相应的另一单元的存在来执行。
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公开(公告)号：US20100119414A1
公开(公告)日：2010-05-13
申请号：US12638347
申请日：2009-12-15
IPC分类号： G01N33/50
CPC分类号： A61B5/14532 , A61B2560/0223 , A61B2560/0475 , A61B2562/0295 , G01N33/48771 , G01N33/48792 , G06F19/00
摘要： A system is provided for measuring an analyte concentration in a body fluid sample, comprising at least one cartridge that contains consumables for multiple measurements, a data carrier which is affixed to the cartridge and contains calibration information for the consumables contained in the cartridge, a hand-held device that comprises a cartridge reception compartment including a reading facility for receiving a cartridge of this type and for reading its data carrier, a measuring facility for measuring the result of a detection reaction, a processor that is connected to the measuring facility and the reading facility for controlling the measuring facility and for analysis of a measuring signal. As an additional system component, at least one replaceable data storage unit is further provided in which supplementary data is stored. The data storage unit functions in combination with calibration information from the data carrier, wherein the hand-held device comprises an interface for transmission of supplementary data from the replaceable data storage unit to the device, and a consumables identification is stored on the data carrier and used by the processor after insertion of a cartridge to determine whether the consumables of the inserted cartridge, combined with the supplementary data that is available to the processor, renders a reliable measurement of an analyte concentration of a body fluid sample feasible.
摘要翻译： 提供了一种用于测量体液样品中的分析物浓度的系统，其包括至少一个包含用于多次测量的消耗品的盒，附接到所述盒的数据载体，并且包含用于所述盒中的消耗品的校准信息，手 所述装置包括盒接收室，所述盒接收室包括用于接收这种类型的盒并用于读取其数据载体的读取装置，用于测量检测反应结果的测量设备，连接到测量设备的处理器和 读取设备，用于控制测量设备和分析测量信号。 作为附加系统组件，还提供至少一个替换数据存储单元，其中存储有补充数据。 数据存储单元与来自数据载体的校准信息组合起来，其中手持设备包括用于将补充数据从可更换数据存储单元传输到设备的接口，并且消耗品标识被存储在数据载体上， 在插入盒之后由处理器使用以确定插入的盒的消耗品是否与处理器可用的补充数据相结合，可以可靠地测量体液样品的分析物浓度。
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公开(公告)号：US07254156B2
公开(公告)日：2007-08-07
申请号：US11038335
申请日：2005-01-19
IPC分类号： H01S3/08
CPC分类号： H01S3/1055 , H01S3/005 , H01S3/08059 , H01S3/0809 , H01S3/0812 , H01S3/094034 , H01S3/213
摘要： A dye-laser includes a resonator formed between two mirrors. The resonator has a longitudinal Z-axis and transverse X- and Y-axes perpendicular to each other and perpendicular to the Z-axis. A beam of laser radiation circulates in the laser resonator generally in a path along the Z-axis. An optical arrangement is provided for expanding the circulating beam in the Y-axis in one circulation direction and correspondingly compressing the expanded beam in the opposite circulation direction. A diffraction grating having rulings parallel to an X-Z plane of the resonator is located in the resonator in the path of the Y-axis expanded beam. The resonator and the diffraction grating are configured and arranged such that the Y-axis expanded beam is incident on the diffraction grating at a compound angle, is diffracted by the diffraction grating onto one of the resonator mirrors, and is reflected by that mirror back onto the grating such that the circulating laser radiation is incident on the diffraction grating twice per round trip in the resonator.
摘要翻译： 染料激光器包括形成在两个反射镜之间的谐振器。 谐振器具有纵向Z轴和垂直于Z轴的垂直X轴和Y轴。 激光束通常在沿着Z轴的路径中在激光谐振器中循环。 提供一种光学装置，用于在一个循环方向上使Y轴上的循环光束膨胀，并相应地沿相反的循环方向压缩扩展光束。 具有与谐振器的X-Z平面平行的法线的衍射光栅位于Y轴扩展光束的路径中的谐振器中。 共振器和衍射光栅被配置和布置成使得Y轴扩展光束以复合角入射在衍射光栅上，被衍射光栅衍射到谐振镜之一上，并被该反射镜反射回 光栅使得循环激光辐射在谐振器中每次往返两次入射到衍射光栅上。
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公开(公告)号：US20060159150A1
公开(公告)日：2006-07-20
申请号：US11038335
申请日：2005-01-19
IPC分类号： H01S3/08
CPC分类号： H01S3/1055 , H01S3/005 , H01S3/08059 , H01S3/0809 , H01S3/0812 , H01S3/094034 , H01S3/213
摘要： A dye-laser includes a resonator formed between two mirrors. The resonator has a longitudinal Z-axis and transverse X- and Y-axes perpendicular to each other and perpendicular to the Z-axis. A beam of laser radiation circulates in the laser resonator generally in a path along the Z-axis. An optical arrangement is provided for expanding the circulating beam in the Y-axis in one circulation direction and correspondingly compressing the expanded beam in the opposite circulation direction. A diffraction grating having rulings parallel to an X-Z plane of the resonator is located in the resonator in the path of the Y-axis expanded beam. The resonator and the diffraction grating are configured and arranged such that the Y-axis expanded beam is incident on the diffraction grating at a compound angle, is diffracted by the diffraction grating onto one of the resonator mirrors, and is reflected by that mirror back onto the grating such that the circulating laser radiation is incident on the diffraction grating twice per round trip in the resonator.
摘要翻译： 染料激光器包括形成在两个反射镜之间的谐振器。 谐振器具有纵向Z轴和垂直于Z轴的垂直X轴和Y轴。 激光束通常在沿着Z轴的路径中在激光谐振器中循环。 提供一种光学装置，用于在一个循环方向上使Y轴上的循环光束膨胀，并相应地沿相反的循环方向压缩扩展光束。 具有与谐振器的X-Z平面平行的法线的衍射光栅位于Y轴扩展光束的路径中的谐振器中。 谐振器和衍射光栅被配置和布置成使得Y轴扩展光束以复合角度入射在衍射光栅上，被衍射光栅衍射到谐振镜之一上，并被该反射镜反射回 光栅使得循环激光辐射在谐振器中每次往返两次入射到衍射光栅上。
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公开(公告)号：US10565170B2
公开(公告)日：2020-02-18
申请号：US12643338
申请日：2009-12-21
申请人： P. Douglas Walling , Juergen Rasch-Menges , Stefan Weinert , Steven Bousamra , Abhishek S. Soni , Christoph Eisenhardt
发明人： P. Douglas Walling , Juergen Rasch-Menges , Stefan Weinert , Steven Bousamra , Abhishek S. Soni , Christoph Eisenhardt
摘要： A structured testing method for diagnostic or therapy support of a patient with a chronic disease and devices thereof are disclosed which implement a structured collection procedure based on a medical use case and/or question which provides at least one or more parameters defining entry criterion, a schedule of events, adherence criterion, and exit criterion. The entry criterion establish conditions needed to be met prior to obtaining biomarker data from the patient. Each event can include one or more of a performance time, patient guidance to perform the event, a request for information from the patient a request for patient action, and a request for collection of biomarker data from the patient. The adherence criterion can be used to assess whether an event performed is acceptable to addressing the medical use case and/or question, and the exit criterion establishes conditions needed to be met prior to exiting the collection procedure.
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公开(公告)号：US08628721B2
公开(公告)日：2014-01-14
申请号：US12638347
申请日：2009-12-15
IPC分类号： G01N33/48
CPC分类号： A61B5/14532 , A61B2560/0223 , A61B2560/0475 , A61B2562/0295 , G01N33/48771 , G01N33/48792 , G06F19/00
摘要： A system is provided for measuring an analyte concentration in a body fluid sample, comprising at least one cartridge that contains consumables for multiple measurements, a data carrier affixed to the cartridge that contains calibration information for the consumables, a hand-held device including a reading facility for receiving a cartridge of this type and for reading its data carrier, a measuring facility for measuring the result of a detection reaction, and a processor for controlling the measuring facility and for analysis of a measuring signal. At least one replaceable data storage unit is further provided in which supplementary data is stored. The data storage unit functions in combination with calibration information from the data carrier and is used by the processor to determine whether the consumables of the inserted cartridge renders a reliable measurement of analyte concentration.
摘要翻译： 提供了一种用于测量体液样品中的分析物浓度的系统，包括至少一个包含用于多次测量的消耗品的盒，固定到所述盒的数据载体，其包含所述消耗品的校准信息，包括读数的手持装置 用于接收这种类型的盒并用于读取其数据载体的设备，用于测量检测反应结果的测量设备，以及用于控制测量设备和用于分析测量信号的处理器。 还提供至少一个可更换数据存储单元，其中存储有补充数据。 数据存储单元与来自数据载体的校准信息组合起来，并由处理器使用以确定插入的盒的消耗品是否可靠地测量分析物浓度。
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8.发明申请MEDICAL DEVICE FOR VISUALLY IMPAIRED USERS AND USERS NOT VISUALLY IMPAIRED 审中-公开用于视觉防护用户的医疗设备和不可视的用户公开(公告)号：US20090286211A1
公开(公告)日：2009-11-19
申请号：US12272147
申请日：2008-11-17
申请人： Christoph Eisenhardt , Dirk Voelkel
发明人： Christoph Eisenhardt , Dirk Voelkel
CPC分类号： G09B21/003 , A61B5/14532 , A61B5/7475
摘要： The present invention refers to a medical device for self testing and monitoring the concentration of analytes in a body fluid, or a blood parameter, or for the controlled administration of therapeutic agents, comprising a connectable, preferably pluggable Braille or Braille-like module for visually impaired users, so that both visually impaired users and users not visually impaired can read the data generated by the medical device and/or control the medical device.
摘要翻译： 本发明涉及一种用于自我测试和监测体液或血液参数中的分析物浓度或用于受控施用治疗剂的医疗装置，其包括用于视觉的可连接的，优选可插拔的盲文或盲文模块 受损的用户，使得视力受损的用户和没有视障者的用户可以读取医疗设备产生的数据和/或控制医疗设备。
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公开(公告)号：US20110112384A1
公开(公告)日：2011-05-12
申请号：US12767579
申请日：2010-04-26
IPC分类号： A61B5/145
CPC分类号： A61B90/98 , A61B5/0002 , A61B5/14532 , A61B5/150022 , A61B5/150175 , A61B5/150305 , A61B5/150358 , A61B5/150412 , A61B5/150503 , A61B5/150786 , A61B5/150793 , A61B5/15087 , A61B5/15113 , A61B5/15117 , A61B5/15146 , A61B5/15151 , A61B5/15163 , A61B5/157 , A61B90/96 , A61B2017/00482 , A61B2090/0811 , A61B2562/08
摘要： The invention proposes a medical system which comprises a central control unit which is set up to display at least one diagnostic measured value using a display element. The medical system also comprises at least one invasive unit, wherein the invasive unit has at least one invasive consumable. The invasive consumable is set up to invasively intervene in a tissue of a patient. The invasive unit has at least one contactlessly readable electronic identifier for storing at least one piece of information. The central control unit is set up to electronically read the at least one piece of information in the electronic identifier. The central control unit and the invasive unit are functionally independent of one another such that the respective function of the central control unit and of the invasive unit can be performed independently of the presence of the respective other unit.
摘要翻译： 本发明提出了一种医疗系统，其包括中央控制单元，其被设置为使用显示元件显示至少一个诊断测量值。 所述医疗系统还包括至少一个侵入性单元，其中所述侵入性单元具有至少一种侵入性消耗品。 侵入性消耗品设置为侵入性地介入患者的组织。 侵入单元具有至少一个用于存储至少一条信息的非接触式可读电子标识符。 中央控制单元设置为电子地读取电子标识符中的至少一条信息。 中央控制单元和侵入单元在功能上彼此独立，使得中央控制单元和侵入单元的相应功能可以独立于相应的另一单元的存在来执行。
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10.发明申请STRUCTURED TESTING METHOD FOR DIAGNOSTIC OR THERAPY SUPPORT OF A PATIENT WITH A CHRONIC DISEASE AND DEVICES THEREOF 审中-公开具有慢性疾病的患者的诊断或治疗支持的结构化测试方法及其装置公开(公告)号：US20100212675A1
公开(公告)日：2010-08-26
申请号：US12643338
申请日：2009-12-21
申请人： P. Douglas Walling , Juergen Rasch-Menges , Stefan Weinert , Steven Bousamra , Abhishek S. Soni , Christoph Eisenhardt
发明人： P. Douglas Walling , Juergen Rasch-Menges , Stefan Weinert , Steven Bousamra , Abhishek S. Soni , Christoph Eisenhardt
IPC分类号： A61B5/00
摘要： A structured testing method for diagnostic or therapy support of a patient with a chronic disease and devices thereof are disclosed which implement a structured collection procedure based on a medical use case and/or question which provides at least one or more parameters defining entry criterion, a schedule of events, adherence criterion, and exit criterion. The entry criterion establish conditions needed to be met prior to obtaining biomarker data from the patient. Each event can include one or more of a performance time, patient guidance to perform the event, a request for information from the patient a request for patient action, and a request for collection of biomarker data from the patient. The adherence criterion can be used to assess whether an event performed is acceptable to addressing the medical use case and/or question, and the exit criterion establishes conditions needed to be met prior to exiting the collection procedure.
摘要翻译： 公开了一种用于慢性疾病患者及其装置的诊断或治疗支持的结构化测试方法，其实现基于医疗用例和/或问题的结构化收集程序，所述医疗用例和/或问题提供至少一个或多个定义入门标准的参数， 事件时间表，遵守标准和退出标准。 进入标准确定在从患者获得生物标志物数据之前需要满足的条件。 每个事件可以包括一个或多个执行时间，用于执行事件的患者指导，来自患者对病人动作的请求的请求以及从患者收集生物标志物数据的请求。 遵守标准可用于评估所执行的事件是否可以接受处理医疗用例和/或问题，退出标准确定在退出收集程序之前需要满足的条件。
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