耐高压经编间隔复合材料检测
GB 51160-2016纤维增强塑料设备和管道工程技术规范
本规范适用于采用缠绕、喷射和手糊工艺成型的整体纤维增强塑料设备和管道的设计、制造、安装和工程质量验收。本规范不适用于下列纤维增强塑料设备和管道的设计：运输槽罐、地埋容器、贮罐和双壁罐；不规则形状(非回转体)的容器、贮罐和塔器；盛装剧毒或放射性化学物质的设备和管道；埋地给排水管道；烟囱和烟道；油气田集输管道。
YY 0989.6-2016手术植入物 有源植入医疗器械 第6部分:治疗快速性心律失常的有源植入医疗器械(包括植入式除颤器)的专用要求
YY 0989的本部分规定了适用于植入式心脏除颤器和用于具有治疗快速性心律失常功能的有源植入医疗器械。本部分规定的试验是型式试验，通过对设备样品的测试来确认其符合性。本部分同样适用于有源植入医疗器械的某些非植入式部分和附件(见注1)。植入式脉冲发生器或电极导线的特性应通过本部分中列述的适当方法或其他方法进行验证，其他方法的准确度应能被证明是等于或优于规定的方法。如有争议，应采用本部分规定的方法。第2部分涵盖了用于治疗心动过缓的有源植入医疗器械的各个方面。
UL 935-2001荧光灯镇流器
1.1 These requirements cover ballasts of the resistance, reactance, and electronic (high frequency) types for use with fluorescent lamps involving a potential of 2500 volts or less in accordance with the National Electrical Code, ANSI/NFPA 70.1.2 A fluorescent-lamp ballast may be determined by investigation to be acceptable for use, in a fixtureor other device, with electric-discharge lamps of other than the fluorescent type.1.3 Fluorescent self ballasted lamps and ballast adaptors are evaluated using the Standard forSelf-Ballasted Lamps and Lamp Adapters, UL 1993. The component ballast is evaluated to requirementsin this Standard.1.4 A product that contains features, characteristics, components, materials, or systems new or different from those covered by the requirements in this standard, and that involves a risk of fire or of electric shockor injury to persons shall be evaluated using appropriate additional component and end-productrequirements to maintain the level of safety as originally anticipated by the intent of this standard. A product whose features, characteristics, components, materials, or systems conflict with specific requirements or provisions of this standard does not comply with this standard. Revision of requirements shall be proposed and adopted in conformance with the methods employed for development, revision, and implementation of this standard.
DIN EN ISO 7218-2014食品和动物饲料的微生物学.微生物学检验的通用要求和导则(ISO 7218-2007+Amd 1-2013).德文版本EN ISO 7218-2007+A1-2013
This standard gives general instructions for carrying out microbiological examinations in accordance with specific standards. To help to ensure the validity of the examinations. To ascertain the general techniques used for conducting the examinations are the same in all labs. To help to achieve homogeneous results.
