醫(yī)用氧氣濃縮器 安全要求檢測(cè)

醫(yī)用氧氣濃縮器 安全要求檢測(cè)項(xiàng)目報(bào)價(jià)？??解決方案？??檢測(cè)周期？??樣品要求？

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GB 28482-2012嬰幼兒安撫奶嘴安全要求

本標(biāo)準(zhǔn)規(guī)定了嬰幼兒安撫奶嘴的術(shù)語(yǔ)和定義、安全要求、測(cè)試方法、包裝方式及產(chǎn)品信息。本標(biāo)準(zhǔn)適用于組裝成為嬰幼兒安撫奶嘴或者功能用作為嬰幼兒安撫奶嘴的產(chǎn)品，市場(chǎng)上作醫(yī)療用途的器具除外。本標(biāo)準(zhǔn)不適用于設(shè)計(jì)供專(zhuān)門(mén)醫(yī)師用作醫(yī)療用途的類(lèi)似產(chǎn)品。例如，那些供涉及皮爾羅賓癥或者早產(chǎn)嬰兒用的類(lèi)似產(chǎn)品。這些特殊的情況在資料性附錄A中已有描述。本標(biāo)準(zhǔn)不適用于喂食用途的奶嘴。

GB/T 33942-2017特種設(shè)備事故應(yīng)急預(yù)案編制導(dǎo)則

本標(biāo)準(zhǔn)規(guī)定了特種設(shè)備事故應(yīng)急預(yù)案(以下簡(jiǎn)稱“應(yīng)急預(yù)案”)的編制程序、主要內(nèi)容、格式和要求。本標(biāo)準(zhǔn)適用于特種設(shè)備安裝、修理、改造、充裝、經(jīng)營(yíng)、使用、檢測(cè)單位(以下簡(jiǎn)稱“單位”)的特種設(shè)備事故應(yīng)急預(yù)案編制工作。

GB 50030-2013氧氣站設(shè)計(jì)規(guī)范

本規(guī)范適用于下列新建、改建、擴(kuò)建的氧氣站及其管道工程設(shè)計(jì):1 采用低溫空氣分離法生產(chǎn)氧、氮、氬等氣態(tài)、液態(tài)產(chǎn)品的氧氣站設(shè)計(jì);2 采用常溫空氣分離法生產(chǎn)氧、氮、氬等氣態(tài)產(chǎn)品的氧氣站的設(shè)計(jì);3 氧、氮、氬等空氣分離液態(tài)產(chǎn)品氣化站房的設(shè)計(jì);4 氧、氮、氬等空氣分離氣態(tài)產(chǎn)品的匯流排間設(shè)計(jì)。

GB 50751-2012醫(yī)用氣體工程技術(shù)規(guī)范

本規(guī)范適用于醫(yī)療衛(wèi)生機(jī)構(gòu)中新建、改建或擴(kuò)建的集中供應(yīng)醫(yī)用氣體工程的設(shè)計(jì)、施工及驗(yàn)收。

YY/T 0893-2023醫(yī)用氣體混合器 獨(dú)立氣體混合器

本文件規(guī)定了預(yù)期用于將氧氣與另一種醫(yī)用氣體混合的獨(dú)立氣體混合器的性能和安全要求。本文件不適用于：a)　每種氣體流量獨(dú)立控制的流量計(jì)組；b)　混合氧氣和周?chē)諝獾莫?dú)立氣體混合器；c)　具有兩個(gè)以上不同氣體進(jìn)氣口的獨(dú)立氣體混合器；d)　與氧氣濃縮器相連的獨(dú)立氣體混合器。

YY/T 1468-2016用于醫(yī)用氣體管道系統(tǒng)的氧氣濃縮器供氣系統(tǒng)

本標(biāo)準(zhǔn)規(guī)定了用于符合ISO 7396-1或GB 50751-2012要求的醫(yī)用氣體管道分配系統(tǒng)的氧氣濃縮器供氣系統(tǒng)的設(shè)計(jì)和安裝要求。本標(biāo)準(zhǔn)僅適用于生產(chǎn)富氧空氣(93%氧)的氧氣濃縮器供氣系統(tǒng)(見(jiàn)4.5.1)。本標(biāo)準(zhǔn)不包括在家中使用的氧氣濃縮器。

TSG 24-2015氧艙安全技術(shù)監(jiān)察規(guī)程

本規(guī)程適用于《特種設(shè)備目錄》規(guī)定范圍內(nèi)的醫(yī)用氧艙、高氣壓艙。

TSG R0006-2014氣瓶安全技術(shù)監(jiān)察規(guī)程

本規(guī)程適用于正常環(huán)境溫度（-40度~60度，注1-1）下使用，公稱容積為0.4L~3000L,公稱工作壓力為0.2Mpa~35Mpa(表壓，下同）且壓力與容積的乘積大于或者等于1.0Mpa，盛裝壓縮氣體，高（低）壓液化氣體，低溫液化氣體，溶解氣體，吸附氣體，標(biāo)準(zhǔn)沸點(diǎn)等于或者低于60度的液體以及混合氣體（兩種或者兩種以上氣體）的無(wú)縫氣瓶，焊接氣瓶，焊接絕熱氣瓶，纏繞氣瓶，內(nèi)部裝有填料的氣瓶以及氣瓶附件。

QJ 20848-2018膠體單推-3生產(chǎn)使用安全要求

本標(biāo)準(zhǔn)規(guī)定了膠體單推-3的一般要求、包裝、清洗、貯存、運(yùn)輸、轉(zhuǎn)注、加注、泄出、應(yīng)急處理、人員安全防護(hù)等過(guò)程的安全要求。本標(biāo)準(zhǔn)適用于膠體單推-3的生產(chǎn)和使用。

SN/T 3838-2014進(jìn)出口安全套中亞硝胺和亞硝基化合物的測(cè)定 質(zhì)譜法

本標(biāo)準(zhǔn)規(guī)定了天然乳膠制安全套中N-亞硝胺和亞硝基化合物測(cè)定的氣相色譜-質(zhì)譜分析方法。本標(biāo)準(zhǔn)適用于天然乳膠制安全套中N-亞硝胺和亞硝基化合物含量的測(cè)定。

DL/T 5311-2013水電水利工程砂石料開(kāi)釆及加工系統(tǒng)運(yùn)行規(guī)范

本標(biāo)準(zhǔn)適用于水電水利工程的特大型、大型、中型砂石系統(tǒng)。

EN 12975-1-2006太陽(yáng)熱能系統(tǒng)和部件.集熱器.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病員用高壓倉(cāng).第4部分:高壓氧氣療法用單人高壓倉(cāng).安全要求和試驗(yàn)

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病員用高壓倉(cāng)(PVHO).高壓療法用多位置高壓室.性能、安全要求和試驗(yàn)

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食品和動(dòng)物飼料的微生物學(xué).微生物學(xué)檢驗(yàn)的通用要求和導(dǎo)則(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.