医用氧气浓缩器 安全要求检测

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GB 28482-2012婴幼儿安抚奶嘴安全要求

本标准规定了婴幼儿安抚奶嘴的术语和定义、安全要求、测试方法、包装方式及产品信息。本标准适用于组装成为婴幼儿安抚奶嘴或者功能用作为婴幼儿安抚奶嘴的产品，市场上作医疗用途的器具除外。本标准不适用于设计供专门医师用作医疗用途的类似产品。例如，那些供涉及皮尔罗宾症或者早产婴儿用的类似产品。这些特殊的情况在资料性附录A中已有描述。本标准不适用于喂食用途的奶嘴。

GB/T 33942-2017特种设备事故应急预案编制导则

本标准规定了特种设备事故应急预案(以下简称“应急预案”)的编制程序、主要内容、格式和要求。本标准适用于特种设备安装、修理、改造、充装、经营、使用、检测单位(以下简称“单位”)的特种设备事故应急预案编制工作。

GB 50030-2013氧气站设计规范

本规范适用于下列新建、改建、扩建的氧气站及其管道工程设计:1 采用低温空气分离法生产氧、氮、氩等气态、液态产品的氧气站设计;2 采用常温空气分离法生产氧、氮、氩等气态产品的氧气站的设计;3 氧、氮、氩等空气分离液态产品气化站房的设计;4 氧、氮、氩等空气分离气态产品的汇流排间设计。

GB 50751-2012医用气体工程技术规范

本规范适用于医疗卫生机构中新建、改建或扩建的集中供应医用气体工程的设计、施工及验收。

YY/T 0893-2023医用气体混合器 独立气体混合器

本文件规定了预期用于将氧气与另一种医用气体混合的独立气体混合器的性能和安全要求。本文件不适用于：a)　每种气体流量独立控制的流量计组；b)　混合氧气和周围空气的独立气体混合器；c)　具有两个以上不同气体进气口的独立气体混合器；d)　与氧气浓缩器相连的独立气体混合器。

YY/T 1468-2016用于医用气体管道系统的氧气浓缩器供气系统

本标准规定了用于符合ISO 7396-1或GB 50751-2012要求的医用气体管道分配系统的氧气浓缩器供气系统的设计和安装要求。本标准仅适用于生产富氧空气(93%氧)的氧气浓缩器供气系统(见4.5.1)。本标准不包括在家中使用的氧气浓缩器。

TSG 24-2015氧舱安全技术监察规程

本规程适用于《特种设备目录》规定范围内的医用氧舱、高气压舱。

TSG R0006-2014气瓶安全技术监察规程

本规程适用于正常环境温度（-40度~60度，注1-1）下使用，公称容积为0.4L~3000L,公称工作压力为0.2Mpa~35Mpa(表压，下同）且压力与容积的乘积大于或者等于1.0Mpa，盛装压缩气体，高（低）压液化气体，低温液化气体，溶解气体，吸附气体，标准沸点等于或者低于60度的液体以及混合气体（两种或者两种以上气体）的无缝气瓶，焊接气瓶，焊接绝热气瓶，缠绕气瓶，内部装有填料的气瓶以及气瓶附件。

QJ 20848-2018胶体单推-3生产使用安全要求

本标准规定了胶体单推-3的一般要求、包装、清洗、贮存、运输、转注、加注、泄出、应急处理、人员安全防护等过程的安全要求。本标准适用于胶体单推-3的生产和使用。

SN/T 3838-2014进出口安全套中亚硝胺和亚硝基化合物的测定 质谱法

本标准规定了天然乳胶制安全套中N-亚硝胺和亚硝基化合物测定的气相色谱-质谱分析方法。本标准适用于天然乳胶制安全套中N-亚硝胺和亚硝基化合物含量的测定。

DL/T 5311-2013水电水利工程砂石料开釆及加工系统运行规范

本标准适用于水电水利工程的特大型、大型、中型砂石系统。

EN 12975-1-2006太阳热能系统和部件.集热器.第1部分:一般要求

This European Standard specifies requirements on durability (including mechanical strength), reliability and safety for liquid heating solar collectors. It also includes provisions for evaluation of conformity to these requirements. It is not applicable to those collectors in which the thermal storage unit is an integral part of the collector to such an extent, that the collection process cannot be separated from the storage process for the purpose of making measurements of these two processes. It is basically applicable to concentrating collectors; thermal performance testing as given in EN 12975-2:2006, 6.3. (quasi dynamic testing) is also applicable to most concentrating collector designs, from stationary non-imaging concentrators as CPCs to high concentrating tracking designs. Collectors that are custom-built (built in, roof integrated collectors that do not comprise factory made modules and are assembled directly on the place of installation) cannot be tested in their actual form for durability, reliability and thermal performance according toThis standard. Instead, a module with the same structure as the ready collector is tested. The module gross area in the case of custom built collectors should be at least 2 m 2 . The test is valid only for larger collectors, than the tested module. For collectors the national and European Guidelines for Structural Planning and overhead glazing are not valid. ThereforeThis standard should be applied for the design of the static of the collector.

DIN 13256-4-2002病员用高压仓.第4部分:高压氧气疗法用单人高压仓.安全要求和试验

The document applies to accessible, oxygen-filled or air-filled oneplace pressure pressure chambers designed for pressures in excess of ambient pressure and employed in human medical installations for therapeutical purposes.#,,#

DIN EN 14931-2006病员用高压仓(PVHO).高压疗法用多位置高压室.性能、安全要求和试验

Pressure chambers for therapeutic use are required for the administration of hyperbaric oxygen therapy and for the treatment of decompression illness. These chambers are made to allow the safe administration of hyperoxic gas mixtures at pressure while avoiding the risks of fire within the chamber and of uncontrolled compression or decompression. This standard is applicable to the performance and safety requirements and their associated test methods for multi-place pressure chambers designed for pressures in excess of ambient atmospheric pressure and employed in medical installations for therapeutic purposes.

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.