BS EN ISO 80601-2-13-2012 Medical electrical equipment Particular requirements for basic safety and essential performance of an anaesthetic workstation《医用电气设备 麻醉工作区的基本安全和基本性能的详细要求》.pdf

《BS EN ISO 80601-2-13-2012 Medical electrical equipment Particular requirements for basic safety and essential performance of an anaesthetic workstation《医用电气设备 麻醉工作区的基本安全和基本性能的详细要求》.pdf》由会员分享，可在线阅读，更多相关《BS EN ISO 80601-2-13-2012 Medical electrical equipment Particular requirements for basic safety and essential performance of an anaesthetic workstation《医用电气设备 麻醉工作区的基本安全和基本性能的详细要求》.pdf（116页珍藏版）》请在麦多课文档分享上搜索。

1、raising standards worldwideNO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBSI Standards PublicationBS EN ISO 80601-2-13:2012Medical electrical equipmentPart 2-13: Particular requirements for basic safety and essentialperformance of an anaesthetic workstationCopyright European

2、Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601-2-13:2012 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN ISO 80601-2-13:2012. It is identical

3、to ISO 80601-2-13:2011. It supersedes BS EN 60601-2-13:2006, BS EN ISO 8835-2:2009, BS EN ISO 8835-3:2009+A1:2010, BS EN ISO 8835-4:2009, and BS EN ISO 8835-5:2009, which are withdrawn.The UK participation in its preparation was entrusted to Technical Committee CH/121/1, Breathing attachments and an

4、aesthetic machines.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2013. Pub

5、lished by BSI Standards Limited 2013.ISBN 978 0 580 77702 8 ICS 11.040.10 Compliance with a British Standard cannot confer immunityfrom legal obligations.This British Standard was published under the authority of the Standards Policy and Strategy Committee on 28 February 2013.Amendments issued since

6、 publicationDate Text affectedCopyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-EUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 80601-2-13 December 2012 ICS 11.040.10 Supe

7、rsedes EN ISO 8835-2:2009, EN ISO 8835-3:2009, EN ISO 8835-4:2009, EN ISO 8835-5:2009, EN 60601-2-13:2006 English Version Medical electrical equipment - Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation (ISO 80601-2-13:2011) Appareils lectrom

8、dicaux - Partie 2-13: Exigences particulires de scurit de base et de performance essentielle pour les systmes danesthsie (ISO 80601-2-13:2011) Medizinische elektrische Gerte - Teil 2-13: Besondere Festlegungen fr die Sicherheit einschlielich der wesentlichen Leistungsmerkmale von Ansthesie-Arbeitspl

9、tzen (ISO 80601-2-13:2011) This European Standard was approved by CEN on 18 November 2012. CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-date l

10、ists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC 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 translation und

11、er the responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the official versions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former

12、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 United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUR

13、OPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG Management Centre: Avenue Marnix 17, B-1000 Brussels 2012 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN ISO 80601-2-13:2012: E Copyright European Committee for Standardization

14、Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601-2-13:2012 EN ISO 80601-2-13:2012 (E) 3 Foreword The text of ISO 80601-2-13:2011 has been prepared by Technical Committee ISO/TC 121 “Anaesthetic andrespiratory equ

15、ipment” of the International Organization for Standardization (ISO) and has been taken over asEN ISO 80601-2-13:2012 by Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment” thesecretariat of which is held by BSI. This European Standard shall be given the status of a national standa

16、rd, either by publication of an identicaltext or by endorsement, at the latest by June 2013, and conflicting national standards shall be withdrawn atthe latest by December 2015. Attention is drawn to the possibility that some of the elements of this document may be the subject of patentrights. CEN a

17、nd/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document supersedes EN ISO 8835-2:2009, EN ISO 8835-3:2009, EN ISO 8835-4:2009,EN ISO 8835-5:2009, EN 60601-2-13:2006. This document has been prepared under a mandate given to CEN by the European Commissi

18、on and theEuropean 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 organisations of the fol

19、lowingcountries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, CzechRepublic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece,Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, No

20、rway, Poland, Portugal,Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO 80601-2-13:2011 has been approved by CEN as a EN ISO 80601-2-13:2012 without anymodification. Copyright European Committee for Standardization Provided by

21、 IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601-2-13:2012EN ISO 80601-2-13:2012 (E) 4 Annex ZA (informative) Relationship between this European Standard and the Essential Requirementsof EU Directive 93/42/EEC This European

22、 Standard has been prepared under a mandate given to CEN by the European Commission and theEuropean Free Trade Association to provide a means to conforming to Essential Requirements of the NewApproach Directive 93/42/EEC, Council Directive of 14 June 1993 on the approximation of the laws of the Memb

23、erStates concerning medical devices” (Medical Device Directive). Once this standard is cited in the Official Journal of the European Union under that Directive and has beenimplemented as a national standard in at least one Member State, compliance with the clauses of this standardgiven in Table ZA.1

24、 confers, within the limits of the scope of this standard, a presumption of conformity with thecorresponding Essential Requirements of that Directive and associated EFTA regulations. Table ZA.1 Correspondence between this European Standard and Directive 93/42/EEC Clause(s)/subclause(s) of this EN Co

25、rresponding essential requirements of Directive93/42/EEC Qualifying remarks/ynotes 201.11.6.8; 201.102.3; 201.104.7 7.2 only the risks to patients during NORMAL USE are addressed 201.11.6.3; 201.11.6.8 7.3 201.7.2.105, 201.7.9.2.14 7.5, 2nd and 3rdparagraph 201.101.4.1.2; 201.11.6.3 7.6 IP classific

26、ation according IEC 60529 is governed by EN 60601-1:2006 201.11.101; 201.104.7 8.1 Easy handling and contamination by the patients are not addressed. 201.11.101 8.6 201.16.9.2.1; 201.16.101;201.101.3; 201.101.4.1201.101.4.2; 201.101.9; 201.102.5; 201.102.9; 201.103.4 to 201.103.7;201.104.4; 201.104.

27、5, 201.104.6; 201.105.4; 201.105.6 9.1 201.9.4; 201.9.4.2.4.3; 201.105.7, 202; 209 9.2 (First and second indents) Clause 202 refers to EN 60601-1-2:2007, Clause 209 refers to EN 60601-1-9:2008 201.11; 201.102.4 9.3 201.12.4.104.1; 201.101.6.1; 201.104.2.2 10.1 Copyright European Committee for Standa

28、rdization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601-2-13:2012 EN ISO 80601-2-13:2012 (E) 5 Clause(s)/subclause(s) of this EN Corresponding essential requirements of Directive93/42/EEC Qualifying remarks/yn

29、otes 201.7.4.2; 10.2 201.7.4.3 10.3 201.14 12.1 EN 62304:2006, 1.4 201.14, 201.14.101 12.1 a) EN 62304:2006, 1.4 201.11.8.102; 201.11.8.103 12.2 201.11.8.102 12.3 201.12.4.104.2; 201.12.4.105; 201.12.4.106; 208 12.4 Clause 208 refers to EN 60601-1-8:2006 202 12.5 Clause 202 refers to EN 60601-1-2:20

30、07 201.9 12.7.1 201.9, 201.9.2.103 12.7.2 201.9, 201.11.8.102 12.7.3 201.15, 201.16, 201.101.4.2.1 12.7.4 Covered by compliance with EN 60601-1:2006, 15.4.1 and 16.9 201.11 12.7.5 EN 60601-1:2006, Clause 11 201.101.4.1.3; 201.101.6.2;201.101.6.3; 201.102.2.1;201.102.2.2; 201.102.10.4;201.104.2.1; 20

31、1.104.5; 201.105.2.1; 201.105.2.2; 12.8.1 201.12.4.104.2; 201.12.4.106;201.12.4.107.1; 201.12.4.107.2;201.12.4.107.3; 201.12.4.109; 201.101.2; 201.101.4.3; 201.102.10: 201.102.10.4;201.104.5; 201.105.5; 201.105.8; 208 12.8.2 201.101.6.1; 201.104.2.1; 12.9 201.7, 201.7.2.104; 201.7.9.1; 201.102.1.1.1

32、 13.1 201.7, 201.7.2.3; 201.7.2.101;201.7.2.103; 201.7.2.107; 201.7.4.2 13.2 201.7.9.1 13.3 a) 201.7.2.101 13.3 e) Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601

33、-2-13:2012EN ISO 80601-2-13:2012 (E) 6 Clause(s)/subclause(s) of this EN Corresponding essential requirements of Directive93/42/EEC Qualifying remarks/ynotes 201.7, 201.7.2.101 13.3 f) The indication that the device is forsingle use must be consistentacross the Community is not addressed in a requir

34、ement. 201.7, 201.7.9.3.102 13.3 i) 201.7, 201.7.2 201.7.2.102, 201.7.2.103, 201.7.2.104201.7.2.107201.7.4.2 201.101.6.1201.102.1.1.2201.102.1.1.3201.102.1.1.4201.102.5.2201.102.5.3201.102.5.4201.102.5.7201.103.1.1201.104.1.1201.104.2.1201.104.6201.105.6 13.3 j) 201.7, 201.7.2.3201.104.1.1 13.3 k) 2

35、01.7.2.101 13.3.l) 201.7.2.102; 201.102.5.2;201.102.5.4; 201.102.5.5;201.102.5.6; 201.103.5; 201.103.6; 201.104.4 13.5 201.7 13.6 a) Covered by compliance with EN 60601-1:2006, 7.9.2 201.7 13.6 b) Covered by compliance with EN 60601-1:2006, 7.9.2 201.7.9.2.1 201.7.9.2.14201.11.8201.11.8.101201.11.8.

36、103201.12.4.102201.12.4.103.3201.12.4.106201.12.4.107.2201.12.4.108201.101.1.1201.101.1.2 201.102.1.2 13.6 c) Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601-2-13

37、:2012 EN ISO 80601-2-13:2012 (E) 7 Clause(s)/subclause(s) of this EN Corresponding essential requirements of Directive93/42/EEC Qualifying remarks/ynotes 201.102.7 201.102.8.2201.102.9.2201.102.9.3201.102.10.3201.103.1.2201.104.1.2201.104.2.1201.104.6201.105.1 201.105.2.2201.105.5 201.7, 201.102.10.

38、1 201.103.3.1.5208.5.2.2 13.6 d) maintenance and frequencycovered by compliance with EN 60601-1:2006, 7.9.2.13 201.7.9.2.14 13.6 f) 201.7 201.7.9.2.14 13.6 h), first paragraph only Covered by compliance with EN 60601-1:2006, 7.9.2 201.7 201.7.9.2.1201.7.9.2.8 13.6 i) Covered by compliance with EN 60

39、601-1:2006, 7.9 201.7.9.2.2 201.7.9.2.14 13.6 k) 201.12.4.103 ; 201.12.4.104.1, 201.12.4.109; 201.101.6.1; 201.104.2.2; 13.6 p) 201.7.9.2.1 13.6 q) Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without lic

40、ense from IHS-,-,-BS EN ISO 80601-2-13:2012EN ISO 80601-2-13:2012 (E) 8 For devices which are also machinery within the meaning of Article 2(a) of Directive 2006/42/EC onMachinery, in accordance with Article 3 of Directive 93/42/EEC the following table ZA.102 details the relevantessential health and

41、 safety requirements of Directive 2006/42/EC on Machinery to the extent to which they aremore specific than essential requirements of Directive 93/42/EEC along with the corresponding clauses of thisEuropean Standard. Table ZA.102, however, does not imply any citation in the OJEU under the machineryd

42、irective and thus does not provide presumption of conformity for the machinery directive. Table ZA.102 Relevant Essential Requirements from Directive 2006/42/EC on machinery thatare addressed by this European Standard (according to article 3 of amended Directive 93/42/EEC) Clause(s)/subclause(s) of

43、this EN EHSR of Directive 2006/42/EC Qualifying remarks/notes 201.9.2.102 1.1.4 201.9.2.103 1.1.8 201.7.4.2 201.9.2201.9.2.104201.101.6.1 201.102.1.1.2201.102.1.1.3201.102.9.2 201.104.1.1201.104.2.1206 208 1.2.2 201.101.3201.101.4.1.1201.101.4.1.2201.101.9201.102.5201.102.8.1201.102.9.1 201.103.4, 2

44、01.103.5; 201.103.6201.103.7201.104.4 201.105.4201.105.6 1.5.4 201.9.2.101 1.6.2 201.8 1.6.3 201.7 201.7.2.106 3.6.2 Covered by compliance with EN 60601-1:2006, 7.2 WARNING: Other requirements and other EU Directives may be applicable to the products falling within thescope of this European Standard

45、. Copyright European Committee for Standardization Provided by IHS under license with CENNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-BS EN ISO 80601-2-13:2012ISO 80601-2-13:2011(E) ISO 2011 All rights reserved iiiContents Page Foreword .v Introductionvi 201.1 S

46、cope, object and related standards.1 201.2 Normative references3 201.3 Terms and definitions .5 201.4 General requirements .9 201.5 General requirements for testing ME EQUIPMENT .11 201.6 Classification of ME EQUIPMENT and ME SYSTEMS 11 201.7 ME EQUIPMENT identification, marking and documents .11 20

47、1.8 Protection against electrical HAZARDS from ME EQUIPMENT.15 201.9 Protection against mechanical HAZARDS of ME EQUIPMENT and ME SYSTEMS16 201.10 Protection against unwanted and excessive radiation HAZARDS 17 201.11 Protection against excessive temperatures and other HAZARDS 17 201.12 Accuracy of c

48、ontrols and instruments and protection against hazardous outputs 19 201.13 HAZARDOUS SITUATIONS and fault conditions24 201.14 PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS (PEMS) .24 201.15 Construction of ME EQUIPMENT.25 201.16 ME SYSTEMS .25 201.17 Electromagnetic compatibility of ME EQUIPMENT AND ME SYSTEMS.26 201.101 Additional requirements for ANAESTHETIC GAS DELIVERY SYSTEMS .26 201.102 Additional requirements for an ANAESTHETIC BREATHING SYSTEM 32 201.103 Additional requirements for an ANAESTHETIC GAS SCAVENGING SYSTEM.39 201.104 Additional requirements for an ANAESTHETIC VAPOUR DELIVER