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141 条记录 (耗时 0.044 秒)

    Container monitoring system
    63.
    发明授权
    Container monitoring system 失效
    集装箱监控系统

    公开(公告)号：US06815206B2

    公开(公告)日：2004-11-09

    申请号：US09742315

    申请日：2000-12-21

    申请人： Szu-Min Lin ,  Su-Syin Wu

    发明人： Szu-Min Lin ,  Su-Syin Wu

    IPC分类号： G01N3100

    CPC分类号： A61L2/208 ,  A61L2/24 ,  A61L2/26 ,  A61L2/28 ,  A61L2202/122 ,  A61L2202/14 ,  Y10T436/196666

    摘要： A sterilization system uses a sterilization process monitoring device which is capable of indicating the efficacy of the sterilization process. To enhance accuracy of the monitoring function, the monitoring device is located in such a fashion that an antimicrobial agent used in the process can only reach the monitor through an area containing the article to be sterilized.

    摘要翻译： 灭菌系统使用能够指示灭菌过程的功效的灭菌过程监测装置。 为了提高监测功能的准确性，监测装置的位置使得该方法中使用的抗微生物剂只能通过包含待消毒制品的区域到达监测器。

    Method and apparatus for measuring the concentration of hydrogen peroxide vapor
    65.
    发明授权
    Method and apparatus for measuring the concentration of hydrogen peroxide vapor 有权
    用于测量过氧化氢蒸汽浓度的方法和装置

    公开(公告)号：US06269680B1

    公开(公告)日：2001-08-07

    申请号：US09337727

    申请日：1999-06-21

    申请人： John F. Prieve ,  Paul Taylor Jacobs ,  Szu-Min Lin ,  Richard B. Timmons

    发明人： John F. Prieve ,  Paul Taylor Jacobs ,  Szu-Min Lin ,  Richard B. Timmons

    IPC分类号： G01N2135

    CPC分类号： A61L2/208 ,  A61L2/24 ,  A61L2/28 ,  G01N21/33 ,  Y10T436/206664

    摘要： An improved apparatus and method for measuring the concentration of hydrogen peroxide vapor or gas in a sterilization chamber. The hydrogen peroxide is measured spectrophotometrically in the ultraviolet region between 200 and 400 nm. Because water vapor does not absorb in the ultraviolet region, it does not interfere with the determination of the concentration of the hydrogen peroxide vapor. Although organic compounds have absorbances in the ultraviolet region, the organic compounds are removed by evacuating the sterilization chamber to low levels before doing the hydrogen peroxide determination. The ultraviolet light source is either a low pressure mercury vapor lamp with an emission at 254 nm or a deuterium lamp with an optical filter selective of 206 nm light. A movable gas cell can be used to measure the hydrogen peroxide concentration at various areas in the sterilization chamber. The measurement system can be combined with a feedback loop to control the concentration of hydrogen peroxide in the sterilization chamber.

    摘要翻译： 一种用于测量灭菌室中过氧化氢蒸汽或气体浓度的改进的装置和方法。 在200和400nm之间的紫外线区域，用分光光度法测量过氧化氢。 由于水蒸汽在紫外线区域不吸收，因此不会影响过氧化氢蒸汽浓度的测定。 虽然有机化合物在紫外线区域具有吸光度，但是在进行过氧化氢测定之前，通过将消毒室排空至低水平来除去有机化合物。 紫外线光源是发射在254nm的低压汞蒸气灯或具有选择性为206nm光的滤光器的氘灯。 可移动气室可用于测量灭菌室中各个区域的过氧化氢浓度。 测量系统可以与反馈回路结合，以控制灭菌室中过氧化氢的浓度。

    Integrated cleaning sterilization process
    66.
    发明授权
    Integrated cleaning sterilization process 失效
    综合清洗灭菌工艺

    公开(公告)号：US06203756B1

    公开(公告)日：2001-03-20

    申请号：US08992478

    申请日：1997-12-17

    申请人： Szu-Min Lin ,  Paul Taylor Jacobs

    发明人： Szu-Min Lin ,  Paul Taylor Jacobs

    IPC分类号： A61L900

    CPC分类号： A61L2/208 ,  A61L2/186 ,  A61L2202/122 ,  A61L2202/17 ,  A61L2202/24

    摘要： A method for cleaning and sterilizing a medical device comprises the steps of: a) placing the device into a container, b) cleaning the device with a cleaning solution, c) rinsing the device with rinse solution, d) treating the device with a liquid sterilant, e) vaporizing the liquid sterilant in the container thereby simultaneously sterilizing and drying the device, and providing a sterile, dry product without further rinsing. The method further comprises retaining a predetermined amount of the liquid sterilant in the container prior to step e). Step e) can be conducted under a diffusion restricted environment, or by reducing pressure to a first predetermined pressure followed by further reducing the first pressure to a predetermined second pressure, or at controlled pump down rate.

    摘要翻译： 一种用于医疗装置的清洁和消毒的方法包括以下步骤：a）将装置放置在容器中，b）用清洁溶液清洁装置，c）用冲洗溶液冲洗装置，d）用液体 消毒剂，e）使容器中的液体灭菌剂蒸发，从而同时对该装置进行灭菌和干燥，并提供无菌干燥的产品，无需进一步漂洗。 该方法还包括在步骤e）之前将预定量的液体灭菌剂保持在容器中。 步骤e）可以在扩散受限的环境下进行，或者通过将压力降低到第一预定压力，然后进一步将第一压力降低到预定的第二压力，或以受控的抽空率进行。