EN ISO 7396-1-2007 2500 Medical gas pipeline systems - Part 1 Pipeline systems for compressed medical gases and vacuum (Incorporates Amendment A3 2013)《医疗气体管道系统 第1部分 压缩医疗气体和真空用管道系统.pdf

1、BRITISH STANDARDBS EN ISO 7396-1:2007+A2:2010 Medical gas pipeline systems Part 1: Pipeline systems for compressed medical gases and vacuumICS 11.040.10g49g50g3g38g50g51g60g44g49g42g3g58g44g55g43g50g56g55g3g37g54g44g3g51g40g53g48g44g54g54g44g50g49g3g40g59g38g40g51g55g3g36g54g3g51g40g53g48g44g55g55g4

2、0g39g3g37g60g3g38g50g51g60g53g44g42g43g55g3g47g36g58BS EN ISO +A3:2013Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 7396-1:2007+A3:2013ISBN 978 0 580 75815 7Amendment

3、s/corrigenda issued since publicationDate Comments30 April 2010 Implementation of ISO amendments 1:2010 and 2:2010 with CEN endorsements A1:2010 and A2:201031 May 2013 Implementation of ISO amendment 3:2013 with CEN endorsement A3:2013This British Standard was published under the authority of the St

4、andards Policy and Strategy Committee on 29 June 2007 The British Standards Institution 2013. Published by BSI Standards Limited 2013National forewordThis British Standard is the UK implementation of EN ISO 7396-1:2007+A3:2013. It is identical to ISO 7396-1:2007, incorporating amendments 1:2010, 2:2

5、010 and 3:2013. It supersedes BS EN ISO 7396-1:2007+A2:2010, which is withdrawn.The start and finish of text introduced or altered by amendment is indicated in the text by tags. Tags indicating changes to ISO text carry the number of the ISO amendment. For example, text altered by ISO amendment 1 is

6、 indicated in the text by .The UK participation in its preparation was entrusted by Technical Committee CH/121, Anaesthetic and respiratory equipment, to Subcommittee CH/121/6, Medical gas supply systems.A list of organizations represented on this subcommittee can be obtained on request to its secre

7、tary.The publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application.Compliance with a British Standard cannot confer immunity from legal obligations.Copyright European Committee for Standardization Provided by IHS under licen

8、se with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-EUROPEAN STANDARDNORME EUROPENNEEUROPISCHE NORMEN ISO 7396-1:2007+A2February 2010ICS 11.040.10 Supersedes EN 737-3:1998 English VersionMedical gas pipeline systems - Part 1: Pipeline systems forcompressed m

9、edical gases and vacuum (ISO 7396-1:2007)Rseaux de distribution de gaz mdicaux - Partie 1:Rseaux de distribution de gaz mdicaux comprims et devide (ISO 7396-1:2007)Rohrleitungssysteme fr medizinische Gase - Teil 1:Rohrleitungenssyteme fr medizinische Druckgase undVakuum (ISO 7396-1:2007)This Europea

10、n Standard was approved by CEN on 24 February 2007.CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this EuropeanStandard the status of a national standard without any alteration. Up-to-date lists and bibliographical references conce

11、rning such nationalstandards may be obtained on application to the CEN Management Centre or to any CEN member.This European Standard exists in three official versions (English, French, German). A version in any other language made by translationunder the responsibility of a CEN member into its own l

12、anguage and notified to the CEN Management Centre has the same status as theofficial versions.CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland,France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, L

13、uxembourg, Malta, Netherlands, Norway, Poland, Portugal,Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMIT EUROPEN DE NORMALISATIONEUROPISCHES KOMITEE FR NORMUNGManagement Centre: rue de Stassart, 36 B-1050 Brussels 2007 CEN All rig

14、hts of exploitation in any form and by any means reservedworldwide for CEN national Members.Ref. No. EN ISO 7396-1:2007: EEN ISO 7396-1:2007+A3March 2013Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted withou

15、t license from IHS-,-,-Foreword This document (EN ISO 7396-1:2007) has been prepared by Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment“, the secretariat of which is held by BSI, in collaboration with Technical Committee ISO/TC 121 “Anaesthetic and respiratory equipment“. This

16、European Standard shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by October 2007, and conflicting national standards shall be withdrawn at the latest by April 2009. This document supersedes EN 737-3:1998. This document ha

17、s been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive(s). For relationship with EU Directive(s), see informative Annex ZA, which is an integral part of this document. According to the CEN/C

18、ENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Lux

19、embourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. Foreword to amendment A1This Amendment (EN ISO 7396-1:2007/A1:2010) has been prepared by Technical Committee ISO/TC 121 “Anaesthetic and respiratory equipment“ in collab

20、oration with Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment” the secretariat of which is held by BSI. This Amendment to the European Standard EN ISO 7396:2007 shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the

21、 latest by July 2010, and conflicting national standards shall be withdrawn at the latest by July 2010. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all su

22、ch patent rights. This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive. For relationship with EU Directive, see informative Annex ZA, which is an integral part of this docu

23、ment. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, I

24、reland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingdom. Endorsement notice The text of ISO 7396-1:2007/Amd 1:2010 has been approved by CEN as a EN ISO 7396-1:2007/A1:2010 without any m

25、odification. BS EN ISO 7396-1:2007+A2:2010EN ISO 7396-1:2007+A2:2010 (E)EN ISO 7396-1:2007/A3:2013 (E) 3 Foreword This document (EN ISO 7396-1:2007/A3:2013) has been prepared by Technical Committee ISO/TC 121 “Anaesthetic and respiratory equipment“ in collaboration with Technical Committee CEN/TC 21

26、5 “Respiratory and anaesthetic equipment” the secretariat of which is held by BSI. This Amendment to the European Standard EN ISO 7396:2007 shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by September 2013, and conflicting

27、 national standards shall be withdrawn at the latest by March 2016. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document has

28、been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive. For relationship with EU Directive, see informative Annex ZA, which is an integral part of this document. According to the CEN-CENELEC I

29、nternal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland

30、, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO 7396-1:2007/Amd 3:2013 has been approved by CEN as EN ISO 7396-1:2007/A3:2013 with

31、out any modification. BS EN ISO 7396-1:2007+A3:2013EN ISO 7396-1:2007+A3:2013Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-iii BS EN ISO 7396-1:2007+A2:2010EN ISO 7396-1:2007+A

32、2:2010 (E)Foreword to amendment A2 This document (EN ISO 7396-1:2007/A2:2010) has been prepared by Technical Committee ISO/TC 121 “Anaesthetic and respiratory equipment“ in collaboration with Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment” the secretariat of which is held by B

33、SI. This Amendment to the European Standard EN ISO 7396:2007 shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by August 2010, and conflicting national standards shall be withdrawn at the latest by August 2010. Attention is

34、drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document has been prepared under a mandate given to CEN by the European Commission and the Eur

35、opean Free Trade Association, and supports essential requirements of EU Directive. For relationship with EU Directive, see informative Annex ZA, which is an integral part of this document. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countr

36、ies are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Sloven

37、ia, Spain, Sweden, Switzerland and the United Kingdom. Endorsement notice The text of ISO 7396-1:2007/Amd 2:2010 has been approved by CEN as a EN ISO 7396-1:2007/A2:2010 without any modification. iii BS EN ISO 7396-1:2007+A2:2010EN ISO 7396-1:2007+A2:2010 (E)Fore ord to amendment A2 This document (E

38、N ISO 7396-1:2007/A2:2010) has been prepared by Technical Committee ISO/TC 121 “Anaesthetic and respiratory equipment“ in collaboration with Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment” the secretariat of which is held by BSI. This Amendment to the European Standard EN ISO

39、7396:2007 shall be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by August 2010, and conflicting national standards shall be withdrawn at the latest by August 2010. Attention is drawn to the possibility that some of the elements

40、of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essentia

41、l requirements of EU Directive. For relationship with EU Directive, see informative Annex ZA, which is an integral part of this document. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard:

42、Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingd

43、om. Endorsement notice The text of ISO 7396-1:2007/Amd 2:2010 has been approved by CEN as a EN ISO 7396-1:2007/A2:2010 without any modification. EN ISO 7396-1:2007/A3:2013 (E) 3 Foreword This document (EN ISO 7396-1:2007/A3:2013) has been prepared by Technical Committee ISO/TC 121 “Anaesthetic and r

44、espiratory equipment“ in collaboration with Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment” the secretariat of which is held by BSI. This Amendment to the European Standard EN ISO 7396:2007 shall be given the status of a national standard, either by publication of an identical

45、 text or by endorsement, at the latest by September 2013, and conflicting national standards shall be withdrawn at the latest by March 2016. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held resp

46、onsible for identifying any or all such patent rights. This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive. For relationship with EU Directive, see informative Annex ZA, w

47、hich is an integral part of this document. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former

48、Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO 7396-1:20

49、07/Amd 3:2013 has been approved by CEN as EN ISO 7396-1:2007/A3:2013 without any modification. BS EN ISO 7396-1:2007+A3:2013EN ISO 7396-1:2007+A3:2013Foreword to amendment A3Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-ivContents Page Introduction . vi 1 Scope . 1 2 Normative references . 2 3 Term