ImageVerifierCode 换一换
格式:PDF , 页数:30 ,大小:315.41KB ,
资源ID:592458      下载积分:10000 积分
快捷下载
登录下载
邮箱/手机:
温馨提示:
快捷下载时,用户名和密码都是您填写的邮箱或者手机号,方便查询和重复下载(系统自动生成)。 如填写123,账号就是123,密码也是123。
特别说明:
请自助下载,系统不会自动发送文件的哦; 如果您已付费,想二次下载,请登录后访问:我的下载记录
支付方式: 支付宝扫码支付 微信扫码支付   
验证码:   换一换

加入VIP,免费下载
 

温馨提示:由于个人手机设置不同,如果发现不能下载,请复制以下地址【http://www.mydoc123.com/d-592458.html】到电脑端继续下载(重复下载不扣费)。

已注册用户请登录:
账号:
密码:
验证码:   换一换
  忘记密码?
三方登录: 微信登录  

下载须知

1: 本站所有资源如无特殊说明,都需要本地电脑安装OFFICE2007和PDF阅读器。
2: 试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓。
3: 文件的所有权益归上传用户所有。
4. 未经权益所有人同意不得将文件中的内容挪作商业或盈利用途。
5. 本站仅提供交流平台,并不能对任何下载内容负责。
6. 下载文件中如有侵权或不适当内容,请与我们联系,我们立即纠正。
7. 本站不保证下载资源的准确性、安全性和完整性, 同时也不承担用户因使用这些下载资源对自己和他人造成任何形式的伤害或损失。

版权提示 | 免责声明

本文(CEN TS 14507-1-2003 Inhalational nitric oxide systems Part 1 Delivery systems《氮氧化物吸入系统 第1部分 输送系统》.pdf)为本站会员(towelfact221)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

CEN TS 14507-1-2003 Inhalational nitric oxide systems Part 1 Delivery systems《氮氧化物吸入系统 第1部分 输送系统》.pdf

1、DRAFT FOR DEVELOPMENT DD CEN/TS 14507-1:2003 Inhalational nitric oxide systems Part 1: Delivery systems ICS 11.040.10 DD CEN/TS 14507-1:2003 This Draft for Development was published under the authority of the Standards Policy and Strategy Committee on 11 April 2003 BSI 11 April 2003 ISBN 0 580 41536

2、 8 National foreword This Draft for Development reproduces verbatim CEN/TS 14507-1:2003. This publication is not to be regarded as a British Standard. It is being issued in the Draft for Development series of publications and is of a provisional nature because nitric oxide is a relatively new medica

3、l gas. It should be applied on this provisional basis, so that information and experience of its practical application may be obtained. Comments arising from the use of this Draft for Development are requested so that UK experience can be reported to the European organization responsible for its con

4、version to a European standard. A review of this publication will be initiated 2 years after its publication by the European organization so that a decision can be taken on its status at the end of its 3-year life. Notification of the start of the review period will be made in an announcement in the

5、 appropriate issue of Update Standards. According to the replies received by the end of the review period, the responsible BSI Committee will decide whether to support the conversion into a European standard, to extend the life of the Technical Specification or to withdraw it. Comments should be sen

6、t in writing to the Secretary of BSI Subcommittee CH/121/1, Breathing attachments and anaesthetic machines, at British Standards House, 389 Chiswick High Road, London W4 4AL, giving the document reference and clause number and proposing, where possible, an appropriate revision of the text. A list of

7、 organizations represented on this committee can be obtained on request to its secretary. Cross-references The British Standards which implement international or European publications referred to in this document may be found in the BSI Catalogue under the section entitled “International Standards C

8、orrespondence Index”, or by using the “Search” facility of the BSI Electronic Catalogue or of British Standards Online. Summary of pages This document comprises a front cover, an inside front cover, the CEN/TS title page, pages 2 to 26, an inside back cover and a back cover. The BSI copyright date d

9、isplayed in this document indicates when the document was last issued. Amendments issued since publication Amd. No. Date CommentsTECHNICALSPECIFICATION SPCIFICATIONTECHNIQUE TECHNISCHESPEZIFIKATION CEN/TS145071 March2003 ICS11.040.10 Englishversion InhalationalnitricoxidesystemsPart1:Deliverysystems

10、 InhalationssystemefrSti ckstoffmonoxidTeil1: Abgabesysteme ThisTechnicalSpecification(CEN/TS)wasapprovedbyCENon02November2002forprovisionalapplication. TheperiodofvalidityofthisCEN/TSislimitedinitiallytothreeyears.AftertwoyearsthemembersofCENwillberequested tosubmittheir comments,particularlyontheq

11、uestionwhethertheCEN/TScanbeconvertedintoaEuropeanStandard. CENmembersarerequiredtoannouncetheexistenceofthisCEN/TSinthesamewayasforanENandtomaketheCEN/TSavailable .It ispermissibletokeepconflictingnationalstandardsinforce(inparalleltotheCEN/TS)untilthefinaldecisionaboutthep ossible conversionoftheC

12、EN/TSintoanENisreached. CENmembersarethenationalstandardsbodiesofAustria,Belgium,CzechRepublic,Denmark,Finland,France,Germany,Greece, Hungary,Iceland,Ireland,Italy,Luxembourg,Malta,Netherlands,Norway,Portugal,Slovakia,Spain,Sweden,SwitzerlandandUn ited Kingdom. EUROPEANCOMMITTEEFORSTANDARDIZATION CO

13、MITEUROPENDENORMALISATION EUROPISCHESKOMITEEFRNORMUNG ManagementCentre:ruedeStassart,36B1050Brussels 2003CEN Allrightsofexploitationinanyformandbyanymeansreserved worldwideforCENnationalMembers. Ref.No.CEN/TS145071:2003ECEN/TS145071:2003(E) 2 Contents Page Foreword. 4 Sectionone General 4 1 Scope 4

14、2 Normativereferences . 5 3 Termsanddefinitionsandterminology. . 6 4 Generalrequirementsandrequirementsfortests 6 4.1 Modificationstoclause3oftheGeneralStandard . 6 4.2 Modificationtoclause4oftheGeneralStandard .7 5 Classification. 7 6 Identification,markinganddocuments . . 7 6.1 Markingontheoutside

15、ofequipmentorequipmentparts . 7 7 PowerInput. . 9 Sectiontwo Environmentalconditions .9 8 Basicsafetycategories . . 9 9 Removableprotectivemeans 9 10 Environmentalconditions . . 9 11 Notused. 9 12 Notused. 9 Sectionthree Protectionagainstelectricalshockhazards 9 13 General . 9 14 Requirementsrelated

16、toclassification . 9 15 Limitationofvoltageand/orenergy 9 16 Enclosuresandprotectivecovers. 10 17 Separation 10 18 Protectiveearthing,functionalearthingandpotentialequalization 10 19 Continuousleakagecurrentandpatientauxiliarycurrent . 10 20 Dielectricstrength . 10 Sectionfour Protectionagainstmecha

17、nicalhazards 10 21 Mechanicalstrength . 10 22 Movingparts. . 11 23 Surfaces,corners,andedges. . 11 24 Stabilityinnormaluse 11 25 Expelledparts. . 11 26 Vibrationandnoise . 11 27 Pneumaticandhydraulicpower 11CEN/TS145071:2003(E) 3 28 Suspendedmasses . . 11 Sectionfive Protectionagainsthazardsfromunwa

18、ntedorexcessiveradiation. 12 29 XRadiation 12 30 Alpha,beta,gamma,neutronradiationandotherparticleradiation 12 31 Microwaveradiation . 12 32 Lightradiation(includinglasers) . . 12 33 Infraredradiation . 12 34 Ultravioletradiation. 12 35 Acousticalenergy(includingultrasonics) . 12 36 Electromagneticc

19、ompatibility . 12 Sectionsix Protectionagainsthazardsofignitionofflammablemixtures 13 Sectionseven Protectionagainstexcessivetemperaturesandothersafetyhazards 13 42 Excessivetemperatures. 13 43R) Fireprevention. . 13 44 Overflow,spillage,leakage,humidity,ingressofliquids,cleaning,sterilizationand di

20、sinfection 13 45 Pressurevesselsandpartssubjecttopressure. 1 4 46Human errors 14 47Electrostatic charges. .14 48Biocompatibility 14 49 Interruptionofthepowersupply. 14 Sectioneight Accuracyofoperationdataandprotectionagainstincorrectoutput . 15 50 Accuracyofoperatingdata 15 51 Protectionagainsthazar

21、dousoutput . 15 Sectionnine Abnormaloperationandfaultconditions Environmentaltests 17 52 Abnormaloperationandfaultconditions 17 53 Environmentaltests 17 Sectionten Constructionalrequirements. 17 54 General. 17 55 Enclosuresandcovers . 17 56 Componentsandgeneralassembly . 17 57 Mainsparts,componentsa

22、ndlayout . 18 58 Protectiveearthing Terminalsandconnections. 19 59 Constructionandlayout . 19 Annexes 22 AnnexAA(informative)Rationale . 23 Bibliography . 26CEN/TS145071:2003(E) 4 Foreword Thisdocument(CEN/TS145071:2003)hasbeenpreparedbyTechnicalCommitteeCEN/TC 215 “Respiratoryandanaestheticequipmen

23、t”,thesecretariatofwhichisheldbyBSI. ThisdocumenthasbeenpreparedunderamandategiventoCENbytheEuropeanCommissionandthe EuropeanFreeTradeAssociation,andsupportsessentialrequirementsofEUDirective(s). CEN/TS14507consistsofthefollowingPartsunderthegeneraltitle“Inhalationalnitricoxidesystems“ Part1Delivery

24、systems Part2Supplysystems AttentionisdrawntotherationalesandguidanceonequipmentforusewithnitricoxidegiveninCR13903 AnnexAAofthisPartofCEN/TS14507isgivenforinformationandcontainsrationalestatementsforthisPart ofCEN/TS14507.TheclauseswhichhavecorrespondingrationalestatementsaremarkedwithR)aftertheir

25、number. AccordingtotheCEN/CENELECInternalRegulations,thenationalstandardsorganizationsofthefollowing countriesareboundtoanouncethisEuropeanStandard:Austria,Belgium,CzechRepublic,Denmark, Finland,France,Germany,Greece,Hungary,Iceland,Ireland,Italy,Luxembourg,Malta,Netherlands, Norway,Portugal,Slovaki

26、a,Spain,Sweden,SwitzerlandandtheUnitedKingdom. Sectionone General 1Scope ThisPartofCEN/TS14507referstoEN606011:1990“MedicalelectricalequipmentPart1:General requirementsforsafety“,asamendedbyitsamendments1(1991)and2(1995).ForbrevityPart1isreferred tointhisPartofCEN/TS14507eitherastheGeneralStandardor

27、astheGeneralrequirements. Thescopegiveninclause1oftheGeneralStandardappliesexceptthat1.1isreplacedbythefollowing: 1.1 ThisPartofCEN/TS14507specifiesparticularrequirementsforinhalationalnitricoxidedeliverysystems andtheirmodules.Itcoversdeviceswhichcanbesuppliedincombinedunits,integratedintoanotherme

28、dical device,forexamplealungventilator,orasindividualdevices. ThisPartofCEN/TS14507addressesthemonitoringofnitricoxideandoxygendeliverytothepatientand minimizationoftheproductionofnitrogendioxide. ThisPartofCEN/TS14507coverstherequirementsforinhalationalnitricoxidedeliverysystemsintendedfor medicalu

29、se,forexample,incriticalcare,anaesthesia,andemergency/transportenvironments. NOTE Itisrecognizedthatfromtimetotimeinnovationsanddesignswillappearthatofferadvantagesand yetarenotcoveredbyspecificsafetyrelateddesignorperformanceaspectsofthisPartofCEN/TS14507; suchinnovationsarenottobediscouraged.Asthe

30、techniquesandtechnologiesintheseinnovations advance,itisessentialthatthesafetyobjectivesofthisPartofCEN/TS14507areconsideredasminimum requirements. Therequirementsofclause1.3oftheGeneralStandardapplywiththefollowingadditions: ThenumberingofclausesandsubclausesofthisPartofCEN/TS14507correspondstothat

31、oftheGeneral Standard.ThechangestothetextoftheGeneralStandardarespecifiedbytheuseofthefollowingwords:CEN/TS145071:2003(E) 5 ReplacementmeansthattheclauseorsubclauseoftheGeneralStandardisreplacedcompletelybythetext ofthisPartofCEN/TS14507. AdditionmeansthatthetextofthisPartofCEN/TS14507isadditionalto

32、therequirementsoftheGeneral Standard. AmendmentmeansthattheclauseorsubclauseoftheGeneralStandardisamendedasindicatedbythe textofthisPartofCEN/TS14507. SubclausesorfigureswhichareadditionaltothoseoftheGeneralStandardarenumberedstartingfrom101. AdditionalannexesareletteredAA,BB,etc.andadditionalitemsa

33、a),bb),etc. ThetermthisStandardisusedtomakereferencetotheGeneralStandardandthisPartofCEN/TS14507 takentogether. Wherethereisnocorrespondingsection,clauseorsubclauseinthisPartofCEN/TS14507,thesection, clauseorsubclauseoftheGeneralStandardapplieswithoutmodification. WhereitisintendedthatanypartoftheGe

34、neralStandard,althoughpossiblyrelevant,isnottobeapplied,a statementtothateffectisgiveninthisPartofCEN/TS14507. 2 Normativereferences ThisTechnicalSpecificationincorporatesbydatedorundatedreference,provisionsfromotherpublications. Thesenormativereferencesarecitedattheappropriateplacesinthetextandthep

35、ublicationsarelisted hereafter.Fordatedreferences,subsequentamendmentsapplytothisTechnicalSpecificationonlywhen incorporatedinitbyamendmentorrevision.Forundatedreferencesthelatesteditionofthepublication referredtoapplies(includingamendments). AppendixLofEN606011:1990applieswiththefollowingadditions:

36、 EN475,Medicaldevices Electricallygeneratedalarmsignals. EN7381:1997+A1:2001,Pressureregulatorsforusewithmedicalgases Part1:Pressureregulatorsand pressureregulatorswithflowmeteringdevices. EN7383:1998+A1: 2001, Pressure regulators for use with medical gases Part3:Pressureregulators integratedwithcyl

37、indervalves. EN739:1998+A1:2001,Lowpressurehoseassembliesforusewithmedicalgases. EN12598,Oxygenmonitorsforpatientbreathingmixtures Particularrequirements. EN13221,Highpressureflexibleconnectionsforusewithmedicalgases. EN60068264:1994, Environmental testing Part2:Testmethods TestFh:Vibration,broadban

38、d random(digitalcontrol)andguidance(IEC60068264:1993+Corrigendum1994. EN606011:1990+A1:1993+A2:1995, Medical electrical equipment Part1:Generalrequirementsfor safety(IEC606011:1998+A1:1991+A2:1995). EN6060112,Medicalelectricalequipment Part1:GeneralRequirementsforsafety2.Collateralstandard: Electrom

39、agneticcompatibility Requirementsandtests(IEC6060112:1993). EN 6100042,Electromagneticcompatibility(EMC)Part4:Testingandmeasurementtechniques Section2:Electrostaticdischargeimmunitytest BasicEMCpublication(IEC6100042:1995).CEN/TS145071:2003(E) 6 CEN/TS145072,Inhalationalnitricoxidesystems Part2:Supp

40、lysystems. ENISO4135,Anaestheticandrespiratoryequipment Vocabulary. IEC6006826:1995,Environmentaltesting Part2:Tests TestFc:Vibration(sinusoidal). IEC60068229:1987,Basicenvironmentaltestingprocedures Part2:Tests TestEbandguidance: Bump. IEC600794,Electricalapparatusforexplosivegasatmospheres Part4:M

41、ethodoftestforignition temperature. 3 Termsanddefinitionsandterminology ForthepurposesofthisTechnicalSpecification,clause2oftheGeneralStandardandENISO4135apply togetherwiththefollowingadditions: 3.1 inhalationalnitricoxidedeliverydevice 1) devicethatcontrolstheadditionofnitricoxidetothebreathinggas

42、NOTE Itcancontrolandindicateflow,concentrationordose. 3.2 inhalationalnitricoxidedeliverysystem 2) systemcomprisingnitricoxidedeliverydevice(s),monitoringandalarmdevice(s) 3.3 inhalationalnitricoxidedeliverysystemmonitoringdevice 3) devicethatdisplaysorindicatesthevaluesofvariablespertinenttothedeli

43、veryofnitricoxide NOTE Suchvariablescanberelatedtoe.g.oxygen,nitricoxideandnitrogendioxide. 4 Generalrequirementsandrequirementsfortests 4.1Modificationstoclause3oftheGeneralStandard Clause3oftheGeneralStandardapplieswiththefollowingadditions: 3.6 Additionalitems aa)shortandopencircuitsofcomponentso

44、rwiringwhichcanincreasetemperatures(seesectionseven); bb)anyfaultwhichisnotdetectedbyintrinsicmeansorbyperiodicinspection(e.g.anoxidantleak)shallbe regardedasanormalconditionandnotasinglefaultcondition; 1) Called“deliverydevice”withinthisPartofEN/TS14507. 2) Called“deliverysystem”withinthisPartofEN/TS14507. 3) Called“monitoringdevice”withinthi

copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
备案/许可证编号:苏ICP备17064731号-1