BS EN ISO 15883-1-2009 Washer-disinfectors - General requirements terms and definitions and tests《洗涤消毒器 一般要求 术语 定义和试验》.pdf
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1、BS EN ISO15883-1:2009ICS 11.080.10NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDWasher-disinfectorsPart 1: General requirements,terms and definitions and tests (ISO15883-1:2006)Licensed Copy: Wang Bin, ISO/EXCHANGE CHINA STANDARDS, 17/12/2009 06:29, Uncontroll
2、ed Copy, (c) BSIThis British Standard was published under the authority of the Standards Policy and Strategy Committee on 31 October 2009 BSI 2009ISBN 978 0 580 66657 5Amendments/corrigenda issued since publicationDate CommentsBS EN ISO 15883-1:2009National forewordThis British Standard is the UK im
3、plementation of EN ISO 15883-1:2009. It is identical to ISO 15883-1:2006. It supersedes BS EN ISO 15883-1:2006 which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee LBI/35, Sterilizers, autoclaves and disinfectors.A list of organizations represented on this
4、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.Compliance with a British Standard cannot confer immunity from legal obligations.Licensed Copy: Wang Bin, I
5、SO/EXCHANGE CHINA STANDARDS, 17/12/2009 06:29, Uncontrolled Copy, (c) BSIEUROPEAN STANDARDNORME EUROPENNEEUROPISCHE NORMEN ISO 15883-1June 2009ICS 11.080.10 Supersedes EN ISO 15883-1:2006 English VersionWasher-disinfectors - Part 1: General requirements, terms anddefinitions and tests (ISO 15883-1:2
6、006)Laveurs dsinfecteurs - Partie 1: Exigences gnrales,termes et dfinitions et essais (ISO 15883-1:2006)Reinigungs-Desinfektionsgerte - Teil 1: AllgemeineAnforderungen, Begriffe und Prfverfahren (ISO 15883-1:2006)This European Standard was approved by CEN on 16 May 2009.CEN members are bound to comp
7、ly 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 concerning such nationalstandards may be obtained on application to the CEN Managemen
8、t 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 language and notified to the CEN Management Centre has the same status as theoffi
9、cial 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, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,Romania, Slovakia, Slove
10、nia, Spain, Sweden, Switzerland and United Kingdom.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMIT EUROPEN DE NORMALISATIONEUROPISCHES KOMITEE FR NORMUNGManagement Centre: Avenue Marnix 17, B-1000 Brussels 2009 CEN All rights of exploitation in any form and by any means reservedworldwide for CEN nationa
11、l Members.Ref. No. EN ISO 15883-1:2009: ELicensed Copy: Wang Bin, ISO/EXCHANGE CHINA STANDARDS, 17/12/2009 06:29, Uncontrolled Copy, (c) BSIBS EN ISO 15883-1:2009EN ISO 15883-1:2009 (E) 3 Foreword The text of ISO 15883-1:2006 has been prepared by Technical Committee ISO/TC 198 “Sterilization of heal
12、th care products” of the International Organization for Standardization (ISO) and has been taken over as EN ISO 15883-1:2009 by Technical Committee CEN/TC 102 “Sterilizers for medical purposes” the secretariat of which is held by DIN. This European Standard shall be given the status of a national st
13、andard, either by publication of an identical text or by endorsement, at the latest by December 2009, and conflicting national standards shall be withdrawn at the latest by March 2010. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent right
14、s. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document supersedes EN ISO 15883-1:2006. This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential req
15、uirements of EC Directive. For relationship with EC 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: Austr
16、ia, Belgium, Bulgaria, 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 Kingdom. Endorsemen
17、t notice The text of ISO 15883-1:2006 has been approved by CEN as a EN ISO 15883-1:2009 without any modification. Licensed Copy: Wang Bin, ISO/EXCHANGE CHINA STANDARDS, 17/12/2009 06:29, Uncontrolled Copy, (c) BSIBS EN ISO 15883-1:2009EN ISO 15883-1:2009 (E) 4 Annex ZA (informative) Relationship bet
18、ween this European Standard and the Essential Requirements of EU Directive 93/42/EEC This European Standard has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association to provide a means of conforming to Essential Requirements of the New Approach
19、 Directive 93/42/EEC on medical devices. Once this standard is cited in the Official Journal of the European Communities under that Directive and has been implemented as a national standard in at least one Member State, compliance with the clauses of this standard given in Table ZA.1 confers, within
20、 the limits of the scope of this standard, a presumption of conformity with the corresponding Essential Requirements of that Directive and associated EFTA regulations. Table ZA.1 Correspondence between this European Standard and Directive 93/42/EEC on medical devices Clauses/subclauses of thisEurope
21、an Standard Essential requirements (ERs)of EU Directive 93/42/EEC Qualifying remarks/Notes 4 1, 4, 3, 6, 7.1, 8.1, 9.1, 7.2, 9.2 5.1 2, 7.3 5.1.3 4 5.1.7 7.5 5.1.8 7.5 5.2 1, 2, 6, 7.1, 7.2, 7.3, 7.5, 8.1, 9.1, 9.2, 9.3, 12.5, 12.6, 12.7.1, 12.7.2, 12.7.3, 12.7.4, 12.7.5, 13.1 The WD shall comply wi
22、th the requirements of IEC 61010-2-045 5.4 7.5 Refers only to leakage 5.4.1.2 7.2, 7.5 5.4.1.3 13.1 5.4.1.5 1, 2 5.4.1.6 1, 2 5.4.1.7 1, 2 5.4.1.8 1, 2 5.4.2 13.1 5.4.3 8.1 5.4.4 8.1 5.4.5.2 2 5.4.5.3 2, 7.5 Licensed Copy: Wang Bin, ISO/EXCHANGE CHINA STANDARDS, 17/12/2009 06:29, Uncontrolled Copy,
23、(c) BSIBS EN ISO 15883-1:2009EN ISO 15883-1:2009 (E) 5 Table ZA.1 (continued) Clauses/subclauses of thisEuropean Standard Essential requirements (ERs)of EU Directive 93/42/EEC Qualifying remarks/Notes 5.5.1 2, 7.2 5.5.2 2 5.7 3, 7.2, 7.3 5.8 2, 12.1, 12.7.5 5.9 3 5.10. 13.2 5.11.1 3 5.11.2 2, 3 5.11
24、.3 2, 3 The choice of process verification system shall be based on a documented risk analysis 5.11.4 2, 3 5.12 3, 12.9 5.13 3 5.14 3 5.15 3 5.16 3 5.17 3 5.18 3 5.19 3 5.20 12.1 5.21 12.1 5.22 2, 3 5.23 3, 13.1 5.24 7.2, 7.5 5.25 7.2, 7.5 5.27 3 5.28 3 Licensed Copy: Wang Bin, ISO/EXCHANGE CHINA ST
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