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    • 6. 发明申请
    • MEDICAL DEVICE FOR DETECTING AT LEAST ONE ANALYTE IN A BODY FLUID
    • 用于检测身体流体中至少一种分析物的医疗设备
    • WO2017134211A1
    • 2017-08-10
    • PCT/EP2017/052360
    • 2017-02-03
    • ROCHE DIABETES CARE GMBHF. HOFFMANN-LA ROCHE AGROCHE DIABETES CARE, INC.
    • WALTER, Helmut
    • A61B5/145A61B5/1486
    • A61B5/14503A61B5/14532A61B5/14865A61B5/6849A61B2560/063A61B2562/166A61B2562/242
    • A medical device (110) for detecting at least one analyte in a body fluidis disclosed. The medical device (110) comprises: - at least one analyte sensor (112) having an insertable portion (114) adapted for at least partially being inserted into a body tissue of a user, - at least one insertion cannula (116), wherein the analyte sensor (112) at least partially is placed inside the insertion cannula (116); - at least one housing (118), wherein the housing (118) comprises at least one sensor compartment (120), wherein the sensor compartment (120) forms a sealed compartment (122) receiving at least the insertable portion (114) of the analyte sensor (112), wherein the sealed compartment (122) comprises at least one detachable upper cap (124) and at least one detachable lower cap (126), wherein the detachable lower cap (126) is configured for detachment before insertion, thereby opening the insertable portion (114) for insertion, wherein the insertion cannula (116) is attached to the detachable upper cap (124), wherein the detachable upper cap (124) is configured for detachment after insertion, thereby removing the insertion cannula (116); and - at least one electronics unit (134), wherein the analyte sensor (112) is operably connected to the electronics unit (134), wherein the electronics unit (134) comprises at least one interconnect device (136) with at least one electronic component (142) attached thereto, wherein the interconnect device (136) fully or partially surrounds the housing (118).
    • 公开了一种用于检测体液中的至少一种分析物的医疗装置(110)。 医疗设备(110)包括: - 至少一个分析物传感器(112),其具有适于至少部分地插入使用者的身体组织中的可插入部分(114); - 至少一个插入套管(116),其中 分析物传感器(112)至少部分地放置在插入套管(116)内; - 至少一个壳体(118),其中所述壳体(118)包括至少一个传感器隔室(120),其中所述传感器隔室(120)形成密封隔室(122),所述隔室至少容纳所述可插入部分 分析物传感器112,其中所述密封隔室122包括至少一个可拆卸上盖124和至少一个可拆卸下盖126,其中所述可拆卸下盖126被构造用于在插入之前脱离, 打开可插入部分(114)以便插入,其中插入套管(116)附接到可拆卸上盖(124),其中可拆卸上盖(124)被构造为在插入后脱离,从而移除插入套管 ); 和至少一个电子单元(134),其中分析物传感器(112)可操作地连接到电子单元(134),其中电子单元(134)包括至少一个互连装置(136),其具有至少一个电子 (142),其中互连装置(136)完全或部分地围绕壳体(118)。
    • 10. 发明申请
    • MEASUREMENT SYSTEM FOR MEASURING THE CONCENTRATION OF AN ANALYTE WITH A SUBCUTANEOUS ANALYTE SENSOR
    • 用于测量分析仪与分析仪分析仪传感器浓度的测量系统
    • WO2016193444A1
    • 2016-12-08
    • PCT/EP2016/062673
    • 2016-06-03
    • ROCHE DIABETES CARE GMBHF. HOFFMANN-LA ROCHE AGROCHE DIABETES CARE, INC.
    • RIEBEL, StefanSCHWENKER, Kai-OliverSCHMITZ, RalfMUEGLITZ, CarstenEISSENLOEFFEL, Thomas
    • G06F19/00A61B5/1495A61B5/1486A61B5/145A61M5/142A61M5/172A61M5/168G01N33/487
    • A61B5/0022A61B5/002A61B5/1451A61B5/14532A61B5/14865A61B5/1495A61B2560/0214A61B2560/0475A61M5/14248A61M5/16827A61M5/1723A61M2005/1726A61M2205/3561A61M2205/3569A61M2205/52A61M2205/8206A61M2230/201G06F19/00G06F19/3468G16H10/60G16H40/40G16H40/63G16H50/20
    • The invention provides for a a medical system comprising a control unit (102) and a medical appliance (104). The medical appliance is a body-worn medical appliance with a subcutaneous portion powered by a first battery. The medical appliance comprises a first wireless communication module and a sensor for measuring an analyte concentration. The control unit comprises a second wireless communication module and a second memory comprising an application partition (138) and a persistent partition (140). The application partition contains a medical application (142) and application data (144). The persistent partition contains archived data (146). The archived data comprises a copy of at least a portion of the application data. The medical application is configured for modifying the application data in the application partition and storing the portion of the application data comprised in the archived data in the persistent partition. The medical data entry comprises the analyte concentration, wherein execution of the medical appliance instructions cause the first processor to: record the analyte concentration using the monitoring system, generate a medical data entry at least partially using the analyte concentration, and transfer the medical data entry to the control unit using the wireless communication channel, wherein the application data comprises the medical data entry. The second memory further contains an operating system, wherein the operating system is operable for de-installing the medical application. The de-installation deletes the application data and preserves the archived data on the persistent partition.
    • 本发明提供一种包括控制单元(102)和医疗器具(104)的医疗系统。 医疗器具是具有由第一电池供电的皮下部分的身体佩戴的医疗器具。 医疗器具包括第一无线通信模块和用于测量分析物浓度的传感器。 控制单元包括第二无线通信模块和包括应用分区(138)和持久分区(140)的第二存储器。 应用程序分区包含医疗应用程序(142)和应用程序数据(144)。 持久分区包含归档数据(146)。 归档数据包括应用数据的至少一部分的副本。 医疗应用被配置用于修改应用程序分区中的应用程序数据,并将包含在归档数据中的应用程序数据的部分存储在永久分区中。 医疗数据输入包括分析物浓度,其中医疗器具指令的执行使得第一处理器使用监测系统记录分析物浓度,至少部分地使用分析物浓度产生医学数据输入,并传送医疗数据项 使用所述无线通信信道发送到所述控制单元,其中所述应用数据包括所述医疗数据条目。 第二存储器还包括操作系统,其中操作系统可操作用于解除医疗应用的安装。 解除安装会删除应用程序数据并保留持久分区上的归档数据。