SAE ARP5602/2 A Guideline for Aerospace Platform Fiber Optic Training and Awareness Education Introduction to Aerospace

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Product Code:SAE ARP5602/2
Title:A Guideline for Aerospace Platform Fiber Optic Training and Awareness Education Introduction to Aerospace Fiber Optics Hands-on Competencies
Issuing Committee:As-3 Fiber Optics And Applied Photonics Committee
Scope:This document establishes training guidelines applicable to fiber optic safety training, technical training and fiber awareness for individuals involved in the manufacturing, installation, support, integration and testing of fiber optic systems.
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【英文标准名称】:StandardPracticeforEvaluatingtheOverpressurizationCharacteristicsofInflatableRestraintCushions
【原文标准名称】:可充气缓冲垫的过压特性评定的标准规范
【标准号】:ASTMD5807-2008
【标准状态】:现行
【国别】:美国
【发布日期】:2008
【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】:D13.20
【标准类型】:(Practice)
【标准水平】:()
【中文主题词】:
【英文主题词】:airbag;bagburst;cushion;inflatablerestraint;rupture;Airbagmaterials/applications;Bagburst;Cushion;Inflatablerestraints;Overpressurization;Rupture/rupturestrength
【摘要】:Thispracticeisintendedtobeageneralguidelineforrepetitivetesting,safeconductoftests,andaccuratedatacollectionforinflatablerestraints.Cushionoverpressurizationtestingmaybeusedfordesignandproductionvalidation,formanufacturingprocesscontrol,forlotacceptance,orforacombinationthereof.Thispracticeconstitutestheconditions,apparatus,andproceduresbywhichinflatablerestraintsarecommonlytestedforcushionoverpressurization.Itisintendedtobeusedasaguidelineinestablishingacushionspecificationorequivalentdocument.Thepracticesinthespecificationmaydeviatefromthepracticesdescribedhereinwhen(basedonexperience)considerationsofequipment,cushiondesign,orotherfactorsdictateotherwise.Thereexistsalargevarietyincushionconfigurationsandequipmentdesigns,obviatingastandardtestmethodforcushionoverpressurization.Therefore,acushionspecificationshouldincorporatethepracticesstatedhereinwhendescribingatestmethodfortestingaspecificcushiongeometryandapparatusdesign.Toensureaccuracyandrepeatability,thespecificationshouldalsoaddressprecisionandbiasinamannerconsistentwithASTMprescribedproceduresandconsistentwiththeparticularcushiongeometry,equipmentinuse,andtestprocedures.Sourcesofvariationincushionoverpressurizationtestingproceduresincludeorificesize,attachmentfixture,sensorlocation,methodofattachment,presenceorabsenceofinternalbladder,accumulatorsizeandpressure,transducertypeandlocation,thepresenceorabsenceoftethers,presenceorabsenceofventplugs,andtheaccuracyoftimingdevicesandpressuresensors.Allsourcesofequipmentandproceduralvariationshouldbeaddressedintheapplicablespecification.Inaccordancewiththeapplicablespecification,cushionsmaybepressurizedwithoutburstingtodeterminetheirresistancetoafixedlevelofhighinternalpressure,ortheymaybesubjectedtoincreasingpressurestodeterminetheirultimateburstingstrength.1.1Thispracticecoverstheproceduresandconditionsusedtoevaluatethephysicalperformanceofinflatablerestraintcushionsduringandafteroverpressurizationtestingatelevatedpressurescapableofcausingcushionburstingusingairpressurizationequipment.1.2Thephysicalperformancecharacteristicsthatmaybeobtainedinconjunctionwiththispracticeareinternalcushionpressuresdeterminedbyinstrumentationandmaterialintegrity,determinedbyvisualinspection.1.3Thispracticeisapplicabletoallinflatablerestraintcushions.1.4Proceduresandapparatusotherthanthosestatedinthispracticemaybeusedbyagreementbetweenpurchaserandsupplierwiththespecificdeviationsfromthispracticeacknowledgedinthereport.1.5ThevaluesstatedineitherSIunitsorinch-poundunitsaretoberegardedseparatelyasstandard.Thevaluesstatedineachsystemarenotexactequivalents;therefore,eachsystemmustbeusedindependentlyoftheother.1.6Thisstandarddoesnotpurporttoaddressallofthesafetyconcerns,ifany,associatedwithitsuse.Itistheresponsibilityoftheuserofthisstandardtoestablishappropriatesafetyandhealthpracticesanddeterminetheapplicabilityofregulatorylimitationspriortouse.SeeSection8forspecifichazardinformation.
【中国标准分类号】:T26
【国际标准分类号】:43_040_80
【页数】:3P.;A4
【正文语种】:英语


【英文标准名称】:Packagingforterminallysterilizedmedicaldevices-Part8:Re-usablesterilizationcontainersforsteamsterilizersconformingtoEN285-Requirementsandtestmethods;EnglishversionofDINEN868-8:2009-09
【原文标准名称】:最终灭菌医疗器械的包装.第8部分:符合EN285标准的蒸气消毒器的可重复使用的消毒罐.试验方法和要求.英文版本DINEN868-8-2009-09
【标准号】:DINEN868-8-2009
【标准状态】:现行
【国别】:德国
【发布日期】:2009-09
【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】:应用;容器;卫生学;检验;作标记;材料;医疗器械;医疗器材;医疗产品;医学科学;医疗技术学;包装件;包装;包装材料;包装试验;产品;可重复使用;安全性;安全性要求;规范(验收);蒸汽灭菌;绝育;灭菌;消毒物品;灭菌器;储存;测试;运输包装;证实
【英文主题词】:Applications;Containers;Hygiene;Inspection;Marking;Materials;Medicaldevices;Medicalequipment;Medicalproducts;Medicalsciences;Medicaltechnology;Packages;Packaging;Packagingmaterial;Packagingtests;Products;Re-usable;Safety;Safetyrequirements;Specification(approval);Steamsterilization;Sterilization(birthcontrol);Sterilization(hygiene);Sterilizedgoods;Sterilizers;Storage;Testing;Transportpacking;Validation
【摘要】:ThispartofEN868providestestmethodsandvaluesforre-usablecontainersusedassterilebarriersystemsthatareintendedtomaintainsterilityofterminallysterilizedmedicaldevicestothepointofuse.ThesecontainersareintendedtobeusedinsteamsterilizersconformingtoEN285.NOTE1Theneedforapackagingmaterialinsidethecontainerisdeterminedbythemanufacturesandusers.ThispartofEN868onlyintroducesperformancerequirementsandtestmethodsthatarespecifictotheproductscoveredbythispartofEN868butdoesnotaddnormodifythegeneralrequirementsspecifiedinENISO11607-1.Assuch,theparticularrequirementsin4.2to4.5canbeusedtodemonstratecompliancewithoneormorebutnotalloftherequirementsofENISO11607-1.NOTE2WhenitisintendedtousethecontainersinasteamsterilizernotconformingtoEN285thesterilizationper-formanceofthecontainerinthespecificsterilizationcycletobeusedisvalidatedbytheuser.Otherattributesofthecontainerarealsoreviewedforcompatibilitywiththesterilizercyclee.g.operatingtemperature.NOTE3Whenadditionalmaterialsareusedinsidethesterilebarriersysteminordertoeasetheorganization,dryingorasepticpresentation(e.g.innerwrap,containerfilter,indicators,packinglists,mats,instrumentorganizersets,traylinersoranadditionalenvelopearoundthemedicaldevice)thenotherrequirements,includingthedeterminationoftheacceptabilityofthesematerialsduringvalidationactivities,mayapply.
【中国标准分类号】:C08
【国际标准分类号】:11_080_30
【页数】:21P.;A4
【正文语种】:英语