JIS G4303-1991 不锈钢棒
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【英文标准名称】:Stainlesssteelbars
【原文标准名称】:不锈钢棒
【标准号】:JISG4303-1991
【标准状态】:作废
【国别】:日本
【发布日期】:1991-11-01
【实施或试行日期】:1991-11-01
【发布单位】:日本工业标准调查会(JISC)
【起草单位】:IronandSteel
【标准类型】:()
【标准水平】:()
【中文主题词】:耐腐蚀钢;不锈钢;钢;棒材;材料(按形状分);金属型材
【英文主题词】:stainlesssteels;corrosion-resistantsteels;steels;bars(materials);materialsbyform;metalsections
【摘要】:
【中国标准分类号】:H44
【国际标准分类号】:77_140_20;77_140_60
【页数】:44P;A4
【正文语种】:日语
【原文标准名称】:不锈钢棒
【标准号】:JISG4303-1991
【标准状态】:作废
【国别】:日本
【发布日期】:1991-11-01
【实施或试行日期】:1991-11-01
【发布单位】:日本工业标准调查会(JISC)
【起草单位】:IronandSteel
【标准类型】:()
【标准水平】:()
【中文主题词】:耐腐蚀钢;不锈钢;钢;棒材;材料(按形状分);金属型材
【英文主题词】:stainlesssteels;corrosion-resistantsteels;steels;bars(materials);materialsbyform;metalsections
【摘要】:
【中国标准分类号】:H44
【国际标准分类号】:77_140_20;77_140_60
【页数】:44P;A4
【正文语种】:日语
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【英文标准名称】:Medicaldevices-Qualitymanagementsystems-Requirementsforregulatorypurposes(ISO13485:2003);GermanversionENISO13485:2003+AC:2007
【原文标准名称】:医疗装置.质量管理体系.调整要求
【标准号】:DINENISO13485-2007
【标准状态】:作废
【国别】:德国
【发布日期】:2007-10
【实施或试行日期】:
【发布单位】:德国标准化学会(DE-DIN)
【起草单位】:
【标准类型】:()
【标准水平】:()
【中文主题词】:售后服务;应用;CE标记;消费者与供货者的关系;定义;交付;交货条件;设计;详细规范;开发;文献;电气工程;架设(施工作业);手册;工业;检验;装配;装置;安装;仪器;国际标准;维修;医疗设备;医疗器械;医疗产品;医学科学;组织;工艺管理;采办;产品设计;生产计划;生产;质量;质量评定系统;质量保证;质量保证体系;质量检查;质量控制;质量改进;质量管理;质量要求;卖货商;服务设施;规范;规范(验收);标准;使用;验证
【英文主题词】:After-salesservices;Applications;Auditing;Bearings;CEmarking;Conduits;Consumer-supplierrelations;Corrrections;Customers;Data;Definitions;Delivery;Deliveryconditions;Design;Detailspecification;Developments;Documentations;Editing;Electricalengineering;Erecting(constructionoperation);Establishment;Evaluations;Handbooks;Handling;Industries;Inspection;Installation;Installations;Instruments;Internationalstandards;Maintenance;Medicaldevices;Medicalequipment;Medicalinstruments;Medicalproducts;Medicalsciences;Methods;Organization;Packages;Planning;Preservation;Preventiveactions;Process;Processmanagement;Procurements;Productdesign;Productplanning;Production;Products;Quality;Qualityassessmentsystems;Qualityassurance;Qualityassurancesystems;Qualityauditing;Qualitycontrol;Qualityimprovement;Qualitymanagement;Qualityrequirements;Responsibility;Returncurrent;Sellers;Services;Shipping;Specification;Specification(approval);Standards;Steeringgear;Storage;Surveillance(approval);Testing;Training;Treatment;Use;Verification
【摘要】:1.1GeneralThisInternationalStandardspecifiesrequirementsforaqualitymanagementsystemwhereanorganizationneedstodemonstrateitsabilitytoprovidemedicaldevicesandrelatedservicesthatconsistentlymeetcustomerrequirementsandregulatoryrequirementsapplicabletomedicaldevicesandrelatedservices.TheprimaryobjectiveofthisInternationalStandardistofacilitateharmonizedmedicaldeviceregulatoryrequirementsforqualitymanagementsystems.Asaresult,itincludessomeparticularrequirementsformedicaldevicesandexcludessomeoftherequirementsofISO9001thatarenotappropriateasregulatoryrequirements.Becauseoftheseexclusions,organizationswhosequalitymanagementsystemsconformtothisInternationalStandardcannotclaimconformitytoISO9001unlesstheirqualitymanagementsystemsconformtoalitherequirementsofISO9001(seeAnnexB).1.2ApplicationAllrequirementsofthisInternationalStandardarespecifictoorganizationsprovidingmedicaldevices,regardlessofthetypeorsizeoftheorganization.Ifregulatoryrequirementspermitexclusionsofdesignanddevelopmentcontrols(see7.3),thiscanbeusedasajustificationfortheirexclusionfromthequalitymanagementsystem.Theseregulationscanprovidealternativearrangementsthataretobeaddressedinthequalitymanagementsystem.ItistheresponsibilityoftheorganizationtoensurethatclaimsofconformitywiththisInternationalStandardreflectexclusionofdesignanddevelopmentcontrols[see4.2.2a)and7.3].Ifanyrequirement(s)inClause7ofthisInternationalStandardis(are)notapplicableduetothenatureofthemedicaldevice(s)forwhichthequalitymanagementsystemisapplied,theorganizationdoesnotneedtoincludesucharequirement(s)initsqualitymanagementsystem[see4.2.2a)].TheprocessesrequiredbythisInternationalStandard,whichareapplicabletothemedicaldevice(s),butwhicharenotperformedbytheorganization,aretheresponsibilityoftheorganizationandareaccountedforintheorganization'squalitymanagementsystem[see4.1a)].InthisInternationalStandardtheterms"ifappropriate'and"whereappropriate~areusedseveraltimes.Whenarequirementisqualifiedbyeitherofthesephrases,itisdeemedtobe"appropriate"unlesstheorganizationcandocumentajustificationotherwise.Arequirementisconsidered"appropriate'ifitisnecessaryinorderfor--theproducttomeetspecifiedrequirements,and/or--theorganizationtocarryoutcorrectiveaction.
【中国标准分类号】:C30
【国际标准分类号】:03_120_10;11_040_01
【页数】:69P.;A4
【正文语种】:德语
【原文标准名称】:医疗装置.质量管理体系.调整要求
【标准号】:DINENISO13485-2007
【标准状态】:作废
【国别】:德国
【发布日期】:2007-10
【实施或试行日期】:
【发布单位】:德国标准化学会(DE-DIN)
【起草单位】:
【标准类型】:()
【标准水平】:()
【中文主题词】:售后服务;应用;CE标记;消费者与供货者的关系;定义;交付;交货条件;设计;详细规范;开发;文献;电气工程;架设(施工作业);手册;工业;检验;装配;装置;安装;仪器;国际标准;维修;医疗设备;医疗器械;医疗产品;医学科学;组织;工艺管理;采办;产品设计;生产计划;生产;质量;质量评定系统;质量保证;质量保证体系;质量检查;质量控制;质量改进;质量管理;质量要求;卖货商;服务设施;规范;规范(验收);标准;使用;验证
【英文主题词】:After-salesservices;Applications;Auditing;Bearings;CEmarking;Conduits;Consumer-supplierrelations;Corrrections;Customers;Data;Definitions;Delivery;Deliveryconditions;Design;Detailspecification;Developments;Documentations;Editing;Electricalengineering;Erecting(constructionoperation);Establishment;Evaluations;Handbooks;Handling;Industries;Inspection;Installation;Installations;Instruments;Internationalstandards;Maintenance;Medicaldevices;Medicalequipment;Medicalinstruments;Medicalproducts;Medicalsciences;Methods;Organization;Packages;Planning;Preservation;Preventiveactions;Process;Processmanagement;Procurements;Productdesign;Productplanning;Production;Products;Quality;Qualityassessmentsystems;Qualityassurance;Qualityassurancesystems;Qualityauditing;Qualitycontrol;Qualityimprovement;Qualitymanagement;Qualityrequirements;Responsibility;Returncurrent;Sellers;Services;Shipping;Specification;Specification(approval);Standards;Steeringgear;Storage;Surveillance(approval);Testing;Training;Treatment;Use;Verification
【摘要】:1.1GeneralThisInternationalStandardspecifiesrequirementsforaqualitymanagementsystemwhereanorganizationneedstodemonstrateitsabilitytoprovidemedicaldevicesandrelatedservicesthatconsistentlymeetcustomerrequirementsandregulatoryrequirementsapplicabletomedicaldevicesandrelatedservices.TheprimaryobjectiveofthisInternationalStandardistofacilitateharmonizedmedicaldeviceregulatoryrequirementsforqualitymanagementsystems.Asaresult,itincludessomeparticularrequirementsformedicaldevicesandexcludessomeoftherequirementsofISO9001thatarenotappropriateasregulatoryrequirements.Becauseoftheseexclusions,organizationswhosequalitymanagementsystemsconformtothisInternationalStandardcannotclaimconformitytoISO9001unlesstheirqualitymanagementsystemsconformtoalitherequirementsofISO9001(seeAnnexB).1.2ApplicationAllrequirementsofthisInternationalStandardarespecifictoorganizationsprovidingmedicaldevices,regardlessofthetypeorsizeoftheorganization.Ifregulatoryrequirementspermitexclusionsofdesignanddevelopmentcontrols(see7.3),thiscanbeusedasajustificationfortheirexclusionfromthequalitymanagementsystem.Theseregulationscanprovidealternativearrangementsthataretobeaddressedinthequalitymanagementsystem.ItistheresponsibilityoftheorganizationtoensurethatclaimsofconformitywiththisInternationalStandardreflectexclusionofdesignanddevelopmentcontrols[see4.2.2a)and7.3].Ifanyrequirement(s)inClause7ofthisInternationalStandardis(are)notapplicableduetothenatureofthemedicaldevice(s)forwhichthequalitymanagementsystemisapplied,theorganizationdoesnotneedtoincludesucharequirement(s)initsqualitymanagementsystem[see4.2.2a)].TheprocessesrequiredbythisInternationalStandard,whichareapplicabletothemedicaldevice(s),butwhicharenotperformedbytheorganization,aretheresponsibilityoftheorganizationandareaccountedforintheorganization'squalitymanagementsystem[see4.1a)].InthisInternationalStandardtheterms"ifappropriate'and"whereappropriate~areusedseveraltimes.Whenarequirementisqualifiedbyeitherofthesephrases,itisdeemedtobe"appropriate"unlesstheorganizationcandocumentajustificationotherwise.Arequirementisconsidered"appropriate'ifitisnecessaryinorderfor--theproducttomeetspecifiedrequirements,and/or--theorganizationtocarryoutcorrectiveaction.
【中国标准分类号】:C30
【国际标准分类号】:03_120_10;11_040_01
【页数】:69P.;A4
【正文语种】:德语
基本信息
| 标准名称： | 工业洗衣机 |
| 英文名称： | Industrial washer-extractors |
| 中标分类： | 轻工、文化与生活用品 >> 轻工机械 >> 其他轻工机械 |
| ICS分类： | 家用和商用设备、文娱、体育 >> 洗衣设备 |
| 替代情况： | QB/T 2323-1997 |
| 发布部门： | 中华人民共和国国家发展和改革委员会 |
| 发布日期： | 2004-08-15 |
| 实施日期： | 2005-01-01 |
| 首发日期： | 1900-01-01 |
| 作废日期： | 1900-01-01 |
| 提出单位： | 中国轻工业联合会 |
| 归口单位： | 全国服装洗涤机械标准化技术委员会 |
| 起草单位： | 上海航星机械(集团)有限公司 |
| 起草人： | 工益平 |
| 出版社： | 中国轻工业出版社 |
| 出版日期： | 2005-01-01 |
| 页数： | 13页 |
| 书号： | 155019.2664 |
适用范围
本标准规定了工业洗衣机及洗涤脱水机的术语、产品分类、要求、试验方法、检验规则和标志、包装、运输、贮存。
本标准适用于工业洗衣机和洗涤脱水机，不涉及干洗机和隧道式洗涤机组
前言
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目录
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引用标准
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所属分类： 轻工 文化与生活用品 轻工机械 其他轻工机械 家用和商用设备 文娱 体育 洗衣设备
