发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms
4.1x00a0;This practice identifies methods for cleaning
Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms
1.1 This test method covers counting and sizing airborne particulate matter 5 m and larger (macroparticles). The sampling areas are specifically
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas
1.1?This test method covers counting and sizing airborne particulate matter 5 ?m and larger (macroparticles). The sampling areas are specifically
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Clean Rooms and Other Dust-Controlled Areas Designed for Electronic and Similar Applications
本文件规定了医疗器械洁净室(区)检验人员的要求及准备工作、技术要求及检验方法。 本文件适用于医疗器械洁净室(区)空气洁净度的检验
1、范围 本文件规定了洁净区智能门禁管理系统的技术要求、试验方法、检验规则、标志、包装、运输、贮存、使用说明书。 本文件适用于洁净区智能门禁管理系统的生产工作。 2、技术要求 本文件规定了洁净区智能门禁管理系统的技术要求。 3、试验方法 本文件规定了洁净区智能门禁管理系统的试验方法
Intelligent access control management system for clean area
本标准规定了医药工业洁净室和洁净区中浮游菌测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区,菌室或局部空气净化区域的浮游菌的测试和环境的验证
Test method for airborne microbe in clean room(zone) of the pharmaceutical industry
本标准规定了医药工业洁净室和洁净区中浮游菌测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区,菌室或菌区域(包括洁净工作台)的浮游菌的测定和环境的验证
Test method for airborne microbe in clean room (area) of the pharmaceutical industry
本标准规定了医药工业洁净室和洁净区中沉降菌的测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区,菌室或菌区域(包括洁净工作台)的沉降菌的测定与环境的验证
Test method for settling microbe in clean room (area) of the pharmaceutical industry
Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms
4.1x00a0;This practice identifies methods for cleaning
Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms
1.1 This test method covers counting and sizing airborne particulate matter 5 m and larger (macroparticles). The sampling areas are specifically
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas
1.1?This test method covers counting and sizing airborne particulate matter 5 ?m and larger (macroparticles). The sampling areas are specifically
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Clean Rooms and Other Dust-Controlled Areas Designed for Electronic and Similar Applications
本文件规定了医疗器械洁净室(区)检验人员的要求及准备工作、技术要求及检验方法。 本文件适用于医疗器械洁净室(区)空气洁净度的检验
1、范围 本文件规定了洁净区智能门禁管理系统的技术要求、试验方法、检验规则、标志、包装、运输、贮存、使用说明书。 本文件适用于洁净区智能门禁管理系统的生产工作。 2、技术要求 本文件规定了洁净区智能门禁管理系统的技术要求。 3、试验方法 本文件规定了洁净区智能门禁管理系统的试验方法
Intelligent access control management system for clean area
本标准规定了医药工业洁净室和洁净区中浮游菌测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区,菌室或局部空气净化区域的浮游菌的测试和环境的验证
Test method for airborne microbe in clean room(zone) of the pharmaceutical industry
本标准规定了医药工业洁净室和洁净区中浮游菌测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区,菌室或菌区域(包括洁净工作台)的浮游菌的测定和环境的验证
Test method for airborne microbe in clean room (area) of the pharmaceutical industry
本标准规定了医药工业洁净室和洁净区中沉降菌的测试条件、测试方法。 本标准适用于医药工业洁净室和洁净区,菌室或菌区域(包括洁净工作台)的沉降菌的测定与环境的验证
Test method for settling microbe in clean room (area) of the pharmaceutical industry