BS EN ISO 11990-1-2014 Lasers and laser-related equipment Determination of laser resistance of tracheal tubes Tracheal tube shaft《激光与激光相关设备 气管套管的激光阻抗测定 气管套管传动轴》.pdf
《BS EN ISO 11990-1-2014 Lasers and laser-related equipment Determination of laser resistance of tracheal tubes Tracheal tube shaft《激光与激光相关设备 气管套管的激光阻抗测定 气管套管传动轴》.pdf》由会员分享,可在线阅读,更多相关《BS EN ISO 11990-1-2014 Lasers and laser-related equipment Determination of laser resistance of tracheal tubes Tracheal tube shaft《激光与激光相关设备 气管套管的激光阻抗测定 气管套管传动轴》.pdf(22页珍藏版)》请在麦多课文档分享上搜索。
1、BSI Standards PublicationBS EN ISO 11990-1:2014Lasers and laser-relatedequipment Determinationof laser resistance of trachealtubesPart 1: Tracheal tube shaftBS EN ISO 11990-1:2014 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN ISO11990-1:2014. It is identical t
2、o ISO 11990-1:2011. It supersedes BS ENISO 11990-1:2011 which is withdrawn.The UK participation in its preparation was entrusted to TechnicalCommittee CPW/172, Optics and Photonics.A list of organizations represented on this committee can beobtained on request to its secretary.This publication does
3、not purport to include all the necessaryprovisions of a contract. Users are responsible for its correctapplication. The British Standards Institution 2014. Published by BSI StandardsLimited 2014ISBN 978 0 580 88582 2ICS 11.040.10; 31.260Compliance with a British Standard cannot confer immunity froml
4、egal obligations.This British Standard was published under the authority of theStandards Policy and Strategy Committee on 30 November 2014.Amendments issued since publicationDate Text affectedEUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 11990-1 October 2014 ICS 11.040.10; 31.260 Supersed
5、es EN ISO 11990-1:2011English Version Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 1: Tracheal tube shaft (ISO 11990-1:2011) Lasers et quipements associs aux lasers - Dtermination de la rsistance au laser des tubes trachaux - Partie 1: Axe des tubes
6、 trachaux (ISO 11990-1:2011) Laser und Laseranlagen - Bestimmung der Laserresistenz von Trachealtuben - Teil 1: Trachealtubusschaft (ISO 11990-1:2011) This European Standard was approved by CEN on 22 October 2014. CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipul
7、ate the conditions for giving this European Standard the status of a national standard without any alteration. Up-to-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 St
8、andard exists in three official versions (English, French, German). A version in any other language made by translation 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 n
9、ational standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania,
10、Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2014 CEN All rights of exploitation in any form and by any
11、means reserved worldwide for CEN national Members. Ref. No. EN ISO 11990-1:2014 EBS EN ISO 11990-1:2014EN ISO 11990-1:2014 (E) 3 Foreword The text of ISO 11990-1:2011 has been prepared by Technical Committee ISO/TC 172 “Optics and photonics” of the International Organization for Standardization (ISO
12、) and has been taken over as EN ISO 11990-1:2014 by Technical Committee CEN/TC 123 “Lasers and photonics” the secretariat of which is held by DIN. This 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 A
13、pril 2015, and conflicting national standards shall be withdrawn at the latest by April 2015. 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
14、rights. This document supersedes EN ISO 11990-1:2011. 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, wh
15、ich 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 Y
16、ugoslav 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 11990-1:20
17、11 has been approved by CEN as EN ISO 11990-1:2014 without any modification. BS EN ISO 11990-1:2014EN ISO 11990-1:2014 (E) 4 Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC (Medical Devices) This European Standard has been p
18、repared 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 Directive 93/42/EEC on Medical Devices. Once this standard is cited in the Official Journal of the European Union und
19、er 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 the limits of the scope of this standard, a presumption of conformity with the corresponding Essential Requirements of that
20、 Directive and associated EFTA regulations. NOTE When an Essential Requirement does not appear in Table ZA.1, it means that it is not addressed by this European Standard. Table ZA.1 Correspondence between this European Standard and Directive 93/42/EEC on Medical Devices Clause(s)/sub-clause(s) of th
21、is European Standard Essential Requirements (ERs) of Directive 93/42/EEC Qualifying remarks/Notes This entire standard 7.1 (first indent only) This standard is intended to provide a test method that will allow an evaluation of the risk of ignition associated with the use of a tracheal tube and laser
22、s during ear, nose and throat surgery as part of the risk assessment as set out in these essential requirements. This entire standard 7.3 This entire standard 9.3 WARNING Other requirements and other EU Directives may be applicable to the product(s) falling within the scope of this standard. BS EN I
23、SO 11990-1:2014ISO 11990-1:2011(E) ISO 2011 All rights reserved iiiContents Page Foreword iv Introduction.v 1 Scope1 2 Normative references1 3 Terms and definitions .1 4 Principle2 5 Significance and use of the test 3 6 Apparatus.3 6.1 Gas supply system3 6.2 Containment box .4 6.3 Smoke evacuation .
24、5 6.4 Lasers and delivery systems5 6.5 Oxygen analyser6 7 Reagents and materials 6 8 Preparation of test specimen .6 9 Preparation of apparatus6 10 Test procedure.7 11 Interpretation of results 8 12 Test report8 Bibliography10 BS EN ISO 11990-1:2014ISO 11990-1:2011(E) iv ISO 2011 All rights reserved
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