DIN EN 1199-1998 饮用水处理用化学品.磷酸二氢二钠

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【英文标准名称】:Chemicalsusedfortreatmentofwaterintendedforhumanconsumption-Disodiumhydrogenorthophosphate;GermanversionEN1199:1997
【原文标准名称】:饮用水处理用化学品.磷酸二氢二钠
【标准号】:DINEN1199-1998
【标准状态】:作废
【国别】:德国
【发布日期】:1998-01
【实施或试行日期】:
【发布单位】:德国标准化学会(DIN)
【起草单位】:
【标准类型】:()
【标准水平】:()
【中文主题词】:试验;磷酸盐;化合物;水;规范(验收);作标记;水质;运输;水常规(实验);药液;杂质;磷酸钠;特性;准备;钠;储存;水处理;饮用水;纯度要求
【英文主题词】:specification(approval);chemicals;purityrequirements;transport;testing;sodium;watertreatment;marking;properties;sodiumphosphate;treatment;phosphates;purification;waterquality;water;storage;potabl
【摘要】:
【中国标准分类号】:G77
【国际标准分类号】:71_100_80
【页数】:9P;A4
【正文语种】:德语


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基本信息
标准名称:SDH微波通信系统测量方法
英文名称:Methods of measurement for SDH microwave communication systems
中标分类: 通信、广播 >> 通信设备 >> 微波通信设备
发布部门:中华人民共和国邮电部
发布日期:1997-03-27
实施日期:1997-07-01
首发日期:1900-01-01
作废日期:1900-01-01
提出单位:邮电部电信科学研究规划院
归口单位:邮电部电信科学研究规划院
起草单位:邮电部第四研究所
起草人:周金满
出版社:人民邮电出版社
出版日期:1997-07-01
页数:14页
适用范围

适用范围:本标准适用于SDH微波通信系统的测量,也可用于室内仿真测量。作室内仿真测量时,系统中所用的部件应该是经过检验的合格产品。

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所属分类: 通信 广播 通信设备 微波通信设备
【英文标准名称】:StandardGuideforCharacterizationandTestingofBiomaterialScaffoldsUsedinTissue-EngineeredMedicalProducts
【原文标准名称】:组织工程医疗产品中使用的生物材料支架的表征和试验用标准指南
【标准号】:ASTMF2150-2007
【标准状态】:现行
【国别】:
【发布日期】:2007
【实施或试行日期】:
【发布单位】:美国材料与试验协会(US-ASTM)
【起草单位】:F04.42
【标准类型】:(Guide)
【标准水平】:()
【中文主题词】:生物技术;医疗产品;医疗技术学;脚手架;测试;组织
【英文主题词】:absorption;bioabsorption;biomaterials;biomedicalmaterial;bioresorption;cellseeding;matrix;porometry;porosimetry;porosity;scaffold;tissueengineering;Biomedicalmaterials/applications;Cellseeding;Impurities--medical/surgicalmaterials/appl
【摘要】:Scaffoldspotentiallymaybemetallic,ceramic,polymeric,natural,orcompositematerials.Scaffoldsareusuallyporoustosomedegree,butmaybesolid.Scaffoldscanrangefrommechanicallyrigidtogelatinousandcanbeeitherabsorbable/degradableornonresorbable/nondegradable.Thescaffoldmayormaynothaveasurfacetreatment.Becauseofthislargebreadthofpossiblestartingmaterialsandscaffoldconstructions,thisguidecannotbeconsideredasexhaustiveinitslistingofpotentiallyapplicabletests.Avoluntaryguidanceforthedevelopmentoftissue-engineeredproductscanbefoundinOmstead,etal(1).GuideF2027containsalistingofpotentiallyapplicabletestmethodsspecifictovariousstartingmaterials.EachTEMPscaffoldproductisuniqueandmayrequiretestingnotwithinthescopeofthisguideorotherguidancedocuments.UsersofthisguideareencouragedtoexaminethereferenceslistedhereinandpertinentFDAorotherregulatoryguidelinesorpractices,andconductaliteraturesearchtoidentifyotherproceduresparticularlypertinentforevaluationoftheirspecificscaffoldmaterial(2,3,4).ItistheultimateresponsibilityoftheTEMPscaffolddesignertodeterminetheappropriatetesting,whetherornotitisdescribedinthisguide.AlistingofpotentiallyapplicabletestsforcharacterizingandanalyzingthematerialsutilizedtofabricatethescaffoldmaybefoundinGuideF2027.However,conformanceofarawmaterialtothisand/oranyothercompendialstandard(s)doesnot,initself,ensurethattheselectedmaterialissuitableorthattheprovidedqualityisadequatetomeettheneedsofaparticularapplication.Thus,othercharacterizationproceduresmayalsoberelevantandnotcoveredbythisguide.ThefollowingprovidesalistingoflinkstoU.S.Foodx0026;DrugAdministration(FDA)x2014;CenterforDevicesx0026;RadiologicHealth(CDRH)websitesthatmaypotentiallycontainadditionalguidancerelevanttobiomaterialscaffoldscoveredwithinthisdocument.RecognizedFDA-CDRHConsensusStandardsDatabase:http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfStandards/search.cfmThisdatabaseprovidesaresourceforlocatingFDArecognizedconsensusstandardsformedicalproducts.FDA-CDRHGoodGuidancePractice(GGP)Database:http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfggp/search.cfmThisdatabaseprovidesaresourceforlocatingnon-bindingFDAguidancedocumentsintendedforCDRHstaff,regulatedindustryandthepublicthatrelatetotheprocessing,content,andevaluationofregulatorysubmissions,thedesign,production,manufacturing,andtestingofregulatedproducts,andFDAinspectionandenforcementprocedures.AdocumentwithinthisdatabasepossessingcontentthatwarrantsparticularconsiderationforitspotentialapplicabilityfortissueengineeringscaffoldsisGuidanceforthePreparationofaPremarketNotificationApplicationforaSurgicalMesh;Final.FDA-CDRHPremarketApproval(PMA)Database:http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMA/pma.cfmFDA-CDRH510(k)(PremarketNotification)Database:http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm1.1Thisguideisaresourceofcurrentlyavailabletestmethodsforthecharacterizationofthecompositionalandstructuralaspectsofbiomaterialscaf......
【中国标准分类号】:C47
【国际标准分类号】:11_020
【页数】:10P.;A4
【正文语种】: