DIN ISO 11040-1-2017 Prefilled syringes - Part 1 Glass cylinders for dental local anaesthetic cartridges (ISO 11040-1 2015)《带药注射器 第1部分 齿科局部麻醉药筒用玻璃筒(ISO 11040-1-2015)》.pdf
《DIN ISO 11040-1-2017 Prefilled syringes - Part 1 Glass cylinders for dental local anaesthetic cartridges (ISO 11040-1 2015)《带药注射器 第1部分 齿科局部麻醉药筒用玻璃筒(ISO 11040-1-2015)》.pdf》由会员分享,可在线阅读,更多相关《DIN ISO 11040-1-2017 Prefilled syringes - Part 1 Glass cylinders for dental local anaesthetic cartridges (ISO 11040-1 2015)《带药注射器 第1部分 齿科局部麻醉药筒用玻璃筒(ISO 11040-1-2015)》.pdf(8页珍藏版)》请在麦多课文档分享上搜索。
1、July 2017 English price group 6No 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 11.040.25!%h)“2692906www.din.deDIN I
2、SO 11040-1Prefilled syringes Part 1: Glass cylinders for dental local anaesthetic cartridges (ISO 110401:2015),English translation of DIN ISO 11040-1:2017-07Vorgefllte Spritzen Teil 1: Glaszylinder fr Dentalkarpulen zur Lokalansthesie (ISO 110401:2015),Englische bersetzung von DIN ISO 11040-1:2017-0
3、7Seringues prremplies Partie 1: Tubes en verre pour cartouches dentaires danesthsie locale (ISO 110401:2015),Traduction anglaise de DIN ISO 11040-1:2017-07SupersedesDIN ISO 110401:199307www.beuth.deDocument comprises 8 pagesDTranslation by DIN-Sprachendienst.In case of doubt, the German-language ori
4、ginal shall be considered authoritative.07.17 A comma is used as the decimal marker. Content Page National foreword 3 National Annex NA (informative) Bibliography 3 Foreword .41 Scope .52 Normative references 53 Dimensions and designation .53.1 Dimensions . 53.2 Designation 64 Requirements 64.1 Mate
5、rial . 64.2 Performance 65 Marking 6Bibliography 8.DIN ISO 11040-1:2017-07 2 National foreword This document (ISO 11040-1:2015) has been prepared by Technical Committee ISO/TC 76 “Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use” with the active
6、participation of German experts. The responsible German body involved in its preparation was DIN-Normenausschuss Medizin (DIN Standards Committee Medicine), Working Committee NA 063-02-03 AA “Packaging systems for loading and application of medical devices”. The DIN Standards corresponding to the In
7、ternational Standards referred to in this document are as follows: ISO 720 DIN ISO 720 ISO 4802-1 DIN ISO 4802-1 ISO 4802-2 DIN ISO 4802-2 Amendments This standard differs from DIN ISO 11040-1:1993-07 as follows: a) gas cylinders of 2,2 ml size have been included; b) requirements on performance and
8、marking have been amended; c) the standard has been editorially revised. Previous editions DIN 58358-1: 1983-06 DIN ISO 11040-1: 1993-07 National Annex NA (informative) Bibliography DIN ISO 720, Glass Hydrolytic resistance of glass grains at 121 C Method of test and classification DIN ISO 4802-1, Gl
9、assware Hydrolytic resistance of the interior surfaces of glass containers Part 1: Determination by titration method and classification DIN ISO 4802-2, Glassware Hydrolytic resistance of the interior surfaces of glass containers Part 2: Determination by flame spectrometry and classification DIN ISO
10、11040-1:2017-07 3 ForewordISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subj
11、ect 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 ISO, also take part in the work. ISO collaborates closely with the International Electrotechnical Commission (IE
12、C) 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, Part 1. In particular the different approval criteria needed for the different types of ISO documents should be n
13、oted. 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 elements of this document may be the subject of patent rights. ISO shall not be held responsible for identifyin
14、g 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 received (see www.iso.org/patents).Any trade name used in this document is information given for the convenience o
15、f 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 adherence to the WTO principles in the Technical Barriers to Trade (TBT) see the following URL: Foreword - Supple
16、mentary information.The committee responsible for this document is ISO/TC 76, Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use.This second edition cancels and replaces the first edition (ISO 11040-1:1992), which has been technically revised with
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