BS EN ISO 21987-2017 Ophthalmic optics Mounted spectacle lenses《眼科光学 安装式眼镜镜片》.pdf
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1、Ophthalmic optics Mounted spectacle lenses(ISO 21987:2017)BS EN ISO 21987:2017BSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06National forewordThis British Standard is the UK implementation of EN ISO 21987:2017. It is identical to ISO 21987:2017. It supersedes BS EN
2、ISO 21987:2009, which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee CH/172/3, Spectacles.A list of organizations represented on this committee can be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 provis
3、ions of a contract. Users are responsible for its correct application. The British Standards Institution 2017 Published by BSI Standards Limited 2017ISBN 978 0 580 89525 8ICS 11.040.70Compliance with a British Standard cannot confer immunity from legal obligations. This British Standard was publishe
4、d under the authority of the Standards Policy and Strategy Committee on 30 September 2017.Amendments/corrigenda issued since publicationDate Text affected BRITISH STANDARDBS EN ISO 21987:2017EUROPEAN STANDARDNORME EUROPENNEEUROPISCHE NORMEN ISO 21987August 2017ICS 11.040.70 Supersedes EN ISO 21987:2
5、009EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMIT EUROPEN DE NORMALISATIONEUROPISCHES KOMITEE FR NORMUNGCEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2017 CEN Ref. No. EN ISO 21987:2017: EAll rights of exploitation in any form and by any means reserved worldwide for CEN national Memb
6、ersOphthalmic optics Mounted spectacle lenses (ISO 21987:2017)Optique ophtalmique Verres ophtalmiques monts (ISO 21987:2017)Augenoptik Fertig montierte Korrektionsbrillenglser (ISO 21987:2017)This European Standard was approved by CEN on 26 May 2017.CEN members are bound to comply with the CEN/CENEL
7、EC Internal Regulations which stipulate 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
8、 to any CEN member.This European Standard 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 offic
9、ial versions.CEN members are the national 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, N
10、orway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom.English VersionEN ISO 21987:2017 (E)European forewordThis document (EN ISO 21987:2017) has been prepared by Technical Committee ISO/TC 172 “Optics and photonics“ in collaboration with
11、Technical Committee CEN/TC 170 “Ophthalmic optics” 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 February 2018, and conflicting national standards shall b
12、e withdrawn at the latest by February 2018.Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN shall not be held responsible for identifying any or all such patent rights.This document supersedes EN ISO 21987:2009.This document ha
13、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.The following referenced
14、 documents are indispensable for the application of this document. For undated references, the latest edition of the referenced document (including any amendments) applies. For dated references, only the edition cited applies. However, for any use of this standard within the meaning of Annex ZA, the
15、 user should always check that any referenced document has not been superseded and that its relevant contents can still be considered the generally acknowledged state-of-art.When an IEC or ISO standard is referred to in the ISO standard text, this shall be understood as a normative reference to the
16、corresponding EN standard, if available, and otherwise to the dated version of the ISO or IEC standard, as listed below.NOTE The way in which these referenced documents are cited in normative requirements determines the extent (in whole or in part) to which they apply.Table Correlation between norma
17、tive references and dated EN and ISO standardsNormative references as listed in Clause 2 of the ISO standardEquivalent dated standardEN ISO or IECISO 7944 EN ISO 7944:1998 + AC:2009 ISO 7944:1998 + Cor.1:2009ISO 8429 EN ISO 8429:1996 ISO 8429:1986ISO 8598-1 EN ISO 8598-1:2014 ISO 8598-1:2014ISO 8624
18、 EN ISO 8624:2011 + A1:2015 ISO 8624:2011+ Amd.1:2015ISO 8980-1 EN ISO 8980-1:2017 ISO 8980-1:2017ISO 8980-2 EN ISO 8980-2:2017 ISO 8980-2:2017ISO 13666 EN ISO 13666:2012 ISO 13666:2012ISO 14889 EN ISO 14889:2013 ISO 14889:2013According to the CEN-CENELEC Internal Regulations, the national standards
19、 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, Ireland, Italy, Latvia, Lithuania, Luxemb
20、ourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom. 2BS EN ISO 21987:2017EN ISO 21987:2017 (E)Endorsement noticeThe text of ISO 21987:2017 has been approved by CEN as EN ISO 21987:2017 without any modific
21、ation.3BS EN ISO 21987:2017EN ISO 21987:2017 (E)Annex ZA (informative) Relationship between this document and the Essential Requirements of Directive 93/42/EEC OJ L 169 aimed to be coveredThis document has been prepared under a Commissions standardization request M/023 concerning the development of
22、European Standards related to medical devices to provide one voluntary means of conforming to essential requirements of Council Directive 93/42/EEC of 14 June 1993 concerning medical devices OJ L 169.Once this standard is cited in the Official Journal of the European Union under that Directive, comp
23、liance with the normative 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 Directive and associated EFTA regulations.NOTE 1 Where a reference from a clause of this
24、standard to the risk management process is made, the risk management process needs to be in compliance with Directive 93/42/EEC as amended by 2007/47/EC. This means that risks have to be reduced as far as possible, to a minimum, to the lowest possible level, minimized or removed, according to the wo
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