EN ISO 13897-2018 en Dentistry - Dental amalgam reusable mixing-capsules.pdf
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1、BSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06Dentistry - Dental amalgam reusable mixing-capsules (ISO 13897:2018)BS EN ISO 13897:2018National forewordThis British Standard is the UK implementation of EN ISO 13897:2018. It is identical to ISO 13897:2018. It superse
2、des BS EN ISO 13897:2004, which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee CH/106/4, Dental Instruments and Equipment.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to
3、include all the necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2018 Published by BSI Standards Limited 2018ISBN 978 0 580 90203 1ICS 11.060.10Compliance with a British Standard cannot confer immunity from legal obligations. Th
4、is British Standard was published under the authority of the Standards Policy and Strategy Committee on 31 March 2018.Amendments/corrigenda issued since publicationDate Text affectedBRITISH STANDARDBS EN ISO 13897:2018EUROPEAN STANDARDNORME EUROPENNEEUROPISCHE NORMEN ISO 13897February 2018ICS 11.060
5、.10 Supersedes EN ISO 13897:2004EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMIT EUROPEN DE NORMALISATIONEUROPISCHES KOMITEE FR NORMUNGCEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2018 CEN Ref. No. EN ISO 13897:2018: EAll rights of exploitation in any form and by any means reserved wo
6、rldwide for CEN national MembersDentistry - Dental amalgam reusable mixing-capsules (ISO 13897:2018)Mdecine bucco-dentaire - Capsules de mlange rutilisables pour amalgame dentaire (ISO 13897:2018)Zahnheilkunde - Wiederverwendbare Mischkapseln fr zahnrztliches Amalgam (ISO 13897:2018)This European St
7、andard was approved by CEN on 2 February 2018.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 lists and bibliographical references concernin
8、g 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 under the responsibility of a CEN member into its
9、 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 Yugoslav Republic of Macedonia, France, Germany
10、, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom.English VersionEN ISO 13897:2018 (E)European forewordThis document (EN ISO 13897:2018) h
11、as been prepared by Technical Committee ISO/TC 106 “Dentistry” in collaboration with Technical Committee CEN/TC 55 “Dentistry” 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
12、, at the latest by August 2018, and conflicting national standards shall be withdrawn at the latest by August 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 p
13、atent rights.This document supersedes EN ISO 13897:2004.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, Fin
14、land, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.Endorsement noticeThe te
15、xt of ISO 13897:2018 has been approved by CEN as EN ISO 13897:2018 without any modification.2BS EN ISO 13897:2018ISO 13897:2018Foreword ivIntroduction v1 Scope . 12 Normative references 13 Terms and definitions . 14 Requirements 24.1 Dimensions . 24.1.1 Length tolerance 24.1.2 Diameter tolerance 24.
16、2 Loss of mass from the mixing-capsule during mixing. 24.3 Retention of dental amalgam in the mixing-capsule 25 Sampling 26 Measurements and test methods 26.1 Dimensions . 26.1.1 Apparatus . 26.1.2 Test sample . 36.1.3 Procedure . 36.1.4 Report 36.2 Loss of mass from the mixing-capsule during mixing
17、. 36.2.1 Principle 36.2.2 Test sample . 36.2.3 Apparatus . 36.2.4 Test procedure . 46.2.5 Expression of the results . 56.2.6 Report 56.3 Retention of dental amalgam in the mixing-capsule 66.3.1 Principle 66.3.2 Test sample . 66.3.3 Apparatus . 66.3.4 Test procedure . 66.3.5 Expression of the results
18、 . 76.3.6 Additional testing 86.3.7 Report 87 Labelling 8Bibliography 9 ISO 2018 All rights reserved iiiContents PageBS EN ISO 13897:2018ISO 13897:2018ForewordISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work
19、 of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmen
20、tal, in liaison with ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.The procedures used to develop this document and those intended for its further maintenance are described in the
21、ISO/IEC Directives, Part 1. In particular the different approval criteria needed for the different types of ISO documents should be noted. This document was drafted in accordance with the editorial rules of the ISO/IEC Directives, Part 2 (see www.iso.org/directives).Attention is drawn to the possibi
22、lity that some of the elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of any patent rights identified during the development of the document will be in the Introduction and/or on the ISO list of p
23、atent declarations received (see www.iso.org/patents).Any trade name used in this document is information given for the convenience of users and does not constitute an endorsement.For an explanation on the voluntary nature of standards, the meaning of ISO specific terms and expressions related to co
24、nformity assessment, as well as information about ISOs adherence to the World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see the following URL: www.iso.org/iso/foreword.html.This document was prepared by Technical Committee ISO/TC 106, Dentistry, Subcommittee SC 6,
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