DIN EN 13976-1-2011 en 4341 Rescue systems - Transportation of incubators - Part 1 Interface conditions German version EN 13976-1 2011《营救系统 婴儿保育箱的运输 第1部分 接口条件 德文版本EN 13976-1-2011》.pdf
《DIN EN 13976-1-2011 en 4341 Rescue systems - Transportation of incubators - Part 1 Interface conditions German version EN 13976-1 2011《营救系统 婴儿保育箱的运输 第1部分 接口条件 德文版本EN 13976-1-2011》.pdf》由会员分享,可在线阅读,更多相关《DIN EN 13976-1-2011 en 4341 Rescue systems - Transportation of incubators - Part 1 Interface conditions German version EN 13976-1 2011《营救系统 婴儿保育箱的运输 第1部分 接口条件 德文版本EN 13976-1-2011》.pdf(14页珍藏版)》请在麦多课文档分享上搜索。
1、August 2011 Translation by DIN-Sprachendienst.English price group 9No part of this translation may be reproduced without prior permission ofDIN Deutsches Institut fr Normung e. V., Berlin. Beuth Verlag GmbH, 10772 Berlin, Germany,has the exclusive right of sale for German Standards (DIN-Normen).ICS
2、11.040.10; 11.160!$snK“1807540www.din.deDDIN EN 13976-1Rescue systems Transportation of incubators Part 1: Interface conditionsEnglish translation of DIN EN 13976-1:2011-08Rettungssysteme Inkubatortransport Teil 1: Anforderungen an SchnittstellenEnglische bersetzung von DIN EN 13976-1:2011-08Systmes
3、 de sauvetage Transport dincubateurs Partie 1: Conditions dinterfaceTraduction anglaise de DIN EN 13976-1:2011-08SupersedesDIN EN 13976-1:2004-03www.beuth.deDocument comprises pagesIn case of doubt, the German-language original shall be considered authoritative.1407.11 DIN EN 13976-1:2011-08 2 A com
4、ma is used as the decimal marker. National foreword This standard has been prepared by Technical Committee CEN/TC 239 “Rescue systems” (Secretariat: DIN, Germany), Working Group WG 4 “Transportation of incubators”. The responsible German body involved in its preparation was the Normenausschuss Rettu
5、ngsdienst und Krankenhaus (Rescue Services and Hospital Standards Committee), Working Committee NA 053-01-02 AA Krankenkraftwagen und deren medizinische und technische Ausstattung. This standard contains specifications meeting the essential requirements set out in EU Directive 93/42/EEC on medical d
6、evices (see Annex ZA). Amendments This standard differs from DIN EN 13976-1:2004-03 as follows: a) normative references have been updated; b) Subclause 4.1.1 “vehicles” has been deleted; c) Subclauses 4.1.2 “Loading” and 4.1.3 “Placement” have been deleted and are now dealt with in DIN EN 13976-2:20
7、11-08; d) Subclause 4.2.4 “General requirements gases (transportation)” has been deleted; the normative references have been included in Subclause 4.1.3 “Gas supply”; e) Annex A “Rationale regarding power use” has been added; f) Annex ZA (informative) concerning the relationship between this Europea
8、n Standard and the essential requirements of EU Directive 93/42/EEC on medical devices has been updated on the basis of EU Directive 2007/47/EC of the European Parliament and of the Council of 5 September 2007 amending Council Directives 90/385/EEC on the approximation of the laws of the Member Stat
9、es relating to active implantable medical devices and 93/42/EEC on medical devices and EU Directive 98/8/EC on the placing on the market of biocidal products; g) the standard has been editorially revised. Previous editions DIN 13072: 1997-01 DIN EN 13976-1: 2004-03 EUROPEAN STANDARD NORME EUROPENNE
10、EUROPISCHE NORM EN 13976-1 May 2011 ICS 11.040.10; 11.160 Supersedes EN 13976-1:2003English Version Rescue systems - Transportation of incubators - Part 1: Interface conditions Systmes de sauvetage - Transport dincubateurs - Partie 1: Conditions dinterface Rettungssysteme - Inkubatortransport - Teil
11、 1: Anforderungen an Schnittstellen This European Standard was approved by CEN on 14 April 2011. 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-
12、date lists 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 translati
13、on under 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, F
14、rance, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE
15、 FR NORMUNG Management Centre: Avenue Marnix 17, B-1000 Brussels 2011 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 13976-1:2011: EEN 13976-1:2011 (E) 2 Contents Page Foreword 3Introduction .41 Scope 52 Normative references 53 Te
16、rms and definitions .64 Requirements .84.1 Interface between transport incubator system and ambulance .84.1.1 Fixation .84.1.2 Electricity 84.1.3 Gas supply 9Annex A (informative) Rationale regarding power use 10Annex ZA (informative) Relationship between this European Standard and the Essential Req
17、uirements of EU Directive 93/42/EEC on medical devices 11Bibliography . 12DIN EN 13976-1:2011-08 EN 13976-1:2011 (E) 3 Foreword This document (EN 13976-1:2011) has been prepared by Technical Committee CEN/TC 239 “Rescue systems”, the secretariat of which is held by DIN. This European Standard shall
18、be given the status of a national standard, either by publication of an identical text or by endorsement, at the latest by November 2011, and conflicting national standards shall be withdrawn at the latest by November 2011. Attention is drawn to the possibility that some of the elements of this docu
19、ment 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 supersedes EN 13976-1:2003. This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Asso
20、ciation, 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. EN 13976-1:2003 has been technically revised. The following points represent the most important changes in the revision: 1) cl
21、arified ambiguous and unclear issues between the two parts (requirements for the transport incubator system interface conditions and system requirements, respectively); 2) proposed items in order to improve fixation, interchangeability and interoperability of the transport incubator system when tran
22、sported in hospitals and between hospitals using different ambulances and air crafts; 3) adapted the standard to developments in neonatal intensive care; 4) excluded proposals on standards for stretchers, vehicles or medical devices. EN 13976 consists of the following parts, under the general title:
23、 Rescue systems Transportation of incubators: Part 1: Interface conditions Part 2: System requirements. 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, Croati
24、a, 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. DIN EN 13976-1:2011-08 EN 1397
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