BS EN ISO 6009-2016 Hypodermic needles for single use Colour coding for identification《皮下注射专用针头 彩色识别编码》.pdf
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1、BS EN ISO 6009:2016Hypodermic needles for singleuse Colour coding foridentificationBSI Standards PublicationWB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 15:06BS EN ISO 6009:2016 BRITISH STANDARDNational forewordThis British Standard is the UK implementation of EN ISO 6009:2016. It supersedes B
2、S EN ISO 6009:1994 which is withdrawn.The UK participation in its preparation was entrusted to Technical Committee CH/84, Catheters and syringes.A list of organizations represented on this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 nece
3、ssary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2016.Published by BSI Standards Limited 2016ISBN 978 0 580 86071 3 ICS 01.070; 11.040.25 Compliance with a British Standard cannot confer immunity from legal obligations.This British
4、Standard was published under the authority of the Standards Policy and Strategy Committee on 30 September 2016.Amendments/corrigenda issued since publicationDate T e x t a f f e c t e dEUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN ISO 6009 August 2016 ICS 11.040.25 Supersedes EN ISO 6009:1994
5、English Version Hypodermic needles for single use - Colour coding for identification (ISO 6009:2016) Aiguilles hypodermiques non rutilisables - Code de couleurs pour lidentification (ISO 6009:2016) Medizinische Einmalkanlen - Farbcodierung zur Identifizierung (ISO 6009:2016) This European Standard w
6、as approved by CEN on 24 August 2016. 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 concerning such n
7、ational 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 own la
8、nguage 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, Gree
9、ce, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey andUnited Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPISCHES KOMITEE FR NORMUNG C
10、EN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels 2016 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN ISO 6009:2016 EBS EN ISO 6009:2016EN ISO 6009:2016 (E) 3 European foreword This document (EN ISO 6009:2016) has be
11、en prepared by Technical Committee ISO/TC 84 “Devices for administration of medicinal products and catheters“ in collaboration with Technical Committee CEN/TC 205 “Non-active medical devices” the secretariat of which is held by DIN. This European Standard shall be given the status of a national stan
12、dard, either by publication of an identical text or by endorsement, at the latest by February 2017, and conflicting national standards shall be withdrawn at the latest by February 2017. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent righ
13、ts. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document supersedes EN ISO 6009:1994. According to the CEN-CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Stand
14、ard: 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, Slovakia, Slovenia, Spa
15、in, Sweden, Switzerland, Turkey and the United Kingdom. Endorsement notice The text of ISO 6009:2016 has been approved by CEN as EN ISO 6009:2016 without any modification. BS EN ISO 6009:2016ISO 6009:2016(E)Foreword ivIntroduction v1 Scope . 12 Terms and definitions . 13 Colour code . 1Annex A (info
16、rmative) Reference colour samples 3Bibliography 6 ISO 2016 All rights reserved iiiContents PageBS EN ISO 6009:2016ISO 6009:2016(E)ForewordISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing Interna
17、tional 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-governmental, in liaison with
18、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 ISO/IEC Directives, P
19、art 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 possibility that some of the
20、 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 patent declarations re
21、ceived (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 meaning of ISO specific terms and expressions related to conformity assessment, as well as information about ISOs a
22、dherence to the WTO principles in the Technical Barriers to Trade (TBT) see the following URL: Foreword - Supplementary information.The committee responsible for this document is ISO/TC 84, Devices for administration of medicinal products and catheters.This fourth edition cancels and replaces the th
23、ird edition (ISO 6009:1992), which has been technically revised. It also incorporates a Technical Corrigendum ISO 6009:1992/Cor.1:2008.The main changes to the previous edition of ISO 6009 introduced by this revision are the following:a) broadening of the range of needles to designated needle size do
24、wn to 0,18 mm;b) review of the use of instrumentally determined colour zones (chromaticity and luminanceindex) as used in previous editions to specify opaque colours and has decided that instrumentalmeasurement is not practicable;c) revision of Annex A;d) deletion of Annex B.iv ISO 2016 All rights r
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