UL 299-2012 干式化学灭火器

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【英文标准名称】:Drychemicalfireextinguishers
【原文标准名称】:干式化学灭火器
【标准号】:UL299-2012
【标准状态】:现行
【国别】:美国
【发布日期】:2012-04-13
【实施或试行日期】:
【发布单位】:美国保险商实验所(US-UL)
【起草单位】:UL
【标准类型】:()
【标准水平】:()
【中文主题词】:
【英文主题词】:Chemicals;Drysubstances;Extinguishingactivity;Extinguishingagents;Fireextinguishers;Fireextinguishingapparatus;Portable
【摘要】:
【中国标准分类号】:C84
【国际标准分类号】:13_220_10
【页数】:
【正文语种】:英语


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【英文标准名称】:Portal,Tower,andPedestalCranes
【原文标准名称】:龙门座起重机、塔式起重机和支架起重机
【标准号】:ANSI/ASMEB30.4-2003
【标准状态】:作废
【国别】:美国
【发布日期】:2003
【实施或试行日期】:
【发布单位】:美国国家标准学会(US-ANSI)
【起草单位】:ANSI
【标准类型】:()
【标准水平】:()
【中文主题词】:桥式起重机;提升装置;安全
【英文主题词】:Bridgecranes;Cranes;Inspection;Installations;Liftingdevices;Liftingequipment;Maintenance;Portalcranes;Power-operated;Safety;Towercranes
【摘要】:Includesprovisionswhichapplytotheconstruction,installation,operation,inspectionandmaintenanceofelectricmotororinternal-combustionenginepoweredportal,tower,andpedestalcranes.
【中国标准分类号】:J80
【国际标准分类号】:53_020_20
【页数】:
【正文语种】:英语


【英文标准名称】:StandardGuideforProcessingCells,Tissues,andOrgansforUseinTissueEngineeredMedicalProducts
【原文标准名称】:组织工程医疗产品中使用的细胞、组织和器官处理的标准指南
【标准号】:ASTMF2210-2002
【标准状态】:现行
【国别】:
【发布日期】:2002
【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】:F04.43
【标准类型】:(Guide)
【标准水平】:()
【中文主题词】:
【英文主题词】:cellandtissueengineering;cells;organs;processingofcells;tissueengineeredmedicalproducts;tissues;tissuesandorgans
【摘要】:Thisguidedescribesthegeneralproductdevelopmentcriteriaandanalysesapplicabletoprocessingofcells,tissues,andorgansusedfortheproductionofTEMPs.Forthepurposesofthisguide,cells,tissues,andorgansmaybederivedfromanyorganismatanydevelopmentalstageandinanystateofhealth.Forexample,thisguideappliestostem,progenitor,somatic,andgermlinecells,aswellascellsfromspecifictissueandorgantypes.Thisguidealsoappliestocells,tissues,andorgansfromhealthy,diseased,orinjuredembryostoadults.Cells,tissues,andorgansmaybecombinedwithascaffoldandmaycontainlocallyorsystemicallyactingbiomoleculesoradrug(medicinal)product.ThistypeofTEMPwouldbeax201C;combinationproduct.x201D;1.1Thisguidedescribestheprocessing,characterization,production,andqualityassuranceofcells,tissues,andorgansusedforTissueEngineeredMedicalProducts(TEMPs).Itconcernsaspectsofprocessingactivitiesforcells,tissues,andorganstobefurtherprocessed.Theseaspectsinclude:(1)cell,tissue,andorganprocessing(thatis,facility,reagents,andproceduresforreceipt,inspection,andstorage;tissueculturecomponents,biologicalriskfactors,andprocessingarea),(2)donors(humanandnonhuman)andscreening,and(3)cell,tissue,andorgancharacterizationandprocessing.1.2ThisguidedoesnotapplytoanymedicalproductsofhumanoriginregulatedbytheU.S.FoodandDrugAdministration(FDA)under21CFRParts16and1270(1)and21CFRParts207,807,and1271(2).1.3Thisstandarddoesnotpurporttoaddressallofthesafetyconcerns,ifany,associatedwithitsuse.Itistheresponsibilityoftheuserofthisstandardtoestablishappropriatesafetyandhealthpracticesanddeterminetheapplicabilityofregulatoryrequirementspriortouse.
【中国标准分类号】:C35
【国际标准分类号】:11_040_01
【页数】:6P.;A4
【正文语种】: