ISO 5841-3-2013 Implants for surgery - Cardiac pacemakers - Part 3 Low-profile connectors (IS-1) for implantable pacemakers《外科植入物 心脏起搏器 第3部分 可植入起搏器用小型连接器(IS-1)》.pdf
《ISO 5841-3-2013 Implants for surgery - Cardiac pacemakers - Part 3 Low-profile connectors (IS-1) for implantable pacemakers《外科植入物 心脏起搏器 第3部分 可植入起搏器用小型连接器(IS-1)》.pdf》由会员分享,可在线阅读,更多相关《ISO 5841-3-2013 Implants for surgery - Cardiac pacemakers - Part 3 Low-profile connectors (IS-1) for implantable pacemakers《外科植入物 心脏起搏器 第3部分 可植入起搏器用小型连接器(IS-1)》.pdf(20页珍藏版)》请在麦多课文档分享上搜索。
1、 ISO 2013 Implants for surgery Cardiac pacemakers Part 3: Low-profile connectors (IS-1) for implantable pacemakers Implants chirurgicaux Stimulateurs cardiaques Partie 3: Connecteurs bas profil (IS-1) pour stimulateurs implantables INTERNATIONAL STANDARD ISO 5841-3 Third edition 2013-04-15 Reference
2、 number ISO 5841-3:2013(E) ISO 5841-3:2013(E)ii ISO 2013 All rights reserved COPYRIGHT PROTECTED DOCUMENT ISO 2013 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including pho
3、tocopying, or posting on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address below or ISOs member body in the country of the requester. ISO copyright office Case postale 56 CH-1211 Geneva 20 Tel. + 41 22 749 01 11 Fax + 41 22 749
4、09 47 E-mail copyrightiso.org Web www.iso.org Published in Switzerland ISO 5841-3:2013(E) ISO 2013 All rights reserved iii Contents Page Foreword iv Introduction v 1 Scope . 1 2 Normative references 1 3 Terms and definitions . 1 4 Requirements 2 4.1 General . 2 4.2 Lead connector . 3 4.3 Connector c
5、avity 4 Annex A (normative) Lead connector electrical impedance test method . 8 Annex B (informative) Rationale .10 ISO 5841-3:2013(E) Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing I
6、nternational 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
7、 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 ISO/IEC Direct
8、ives, 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. www.iso.org/directives Attention is drawn to the possibility that some of t
9、he 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
10、received. 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. The committee responsible for this document is ISO/TC 150, Implants for surgery, Subcommittee SC 6, Active implants. This third edition cancels
11、 and replaces the second edition (ISO 5841-3:2000), which has been technically revised. It also incorporates the Technical Corrigendum ISO 5841-3:2000/Cor 1:2003. ISO 5841 consists of the following parts, under the general title Implants for surgery Cardiac pacemakers: Part 2: Reporting of clinical
12、performance of populations of pulse generators or leads Part 3: Part 3: Low-profile connectors (IS-1) for implantable pacemakersiv ISO 2013 All rights reserved ISO 5841-3:2013(E) Introduction The development of this part of ISO 5841 was prompted by the concern of clinicians over the variety of appar
13、ently similar but incompatible pacing leads of the low-profile in-line type. (Because the major diameter of such leads is 3,2 mm, these connectors were frequently referred to as “3,2 mm” leads.) The purpose of this part of ISO 5841 is to specify a standard connector assembly, IS-1, to allow leads an
14、d pulse generators from different manufacturers to be interchangeable. The safety, reliability and function of a particular connector part are the responsibility of the manufacturer. Annex A gives a test method for lead connector impedance. Annex B provides a rationale: it is recommended that this a
15、nnex be read before using this part of ISO 5841 so that the user is informed about its limited objectives. ISO 2013 All rights reserved v Implants for surgery Cardiac pacemakers Part 3: Low-profile connectors (IS-1) for implantable pacemakers WARNING Do not use the connector cavity specified in this
16、 part of ISO 5841 if the implantable pulse generator is capable of introducing dangerous nonpacing signals (e.g. defibrillation signals) through an IS-1 connector (see 4.3.3). 1 Scope This part of ISO 5841 specifies a connector assembly to be used to connect implantable pacemaker leads to implantabl
17、e pacemaker pulse generators. Essential dimensions and performance requirements related to connector fit are specified, together with appropriate test methods. Other connector features such as fastening means and materials are not specified in this part of ISO 5841. This part of ISO 5841 is applicab
18、le only to the form and fit of the connector assembly, and does not address all aspects of functional compatibility, system performance or reliability of different leads and pulse generator assemblies. This part of ISO 5841 supplements ISO 14708-2 only for those pacemaker components which are claime
19、d by their labelling to be fitted with an IS-1 connector assembly part. It does not replace any requirements in ISO 14708-2. NOTE Pacemaker connector assemblies not complying with this part of ISO 5841 may be safe and reliable and may have clinical advantages. 2 Normative references The following do
20、cuments, in whole or in part, are normatively referenced in this document and are indispensable for its application. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. ISO 14708-2, Implants f
21、or surgery Active implantable medical devices Part 2: Cardiac pacemakers 3 Terms and definitions For the purposes of this document, the terms and definitions given in ISO 14708-2 and the following apply. 3.1 connector assembly assembly consisting of a lead connector and a connector cavity for the el
22、ectrical and mechanical connection of a lead to a pulse generator 3.2 lead connector that part of the connector assembly attached to a lead Note 1 to entry: See Figure 1. INTERNATIONAL ST ANDARD ISO 5841-3:2013(E) ISO 2013 All rights reserved 1 ISO 5841-3:2013(E) 3.3 connector cavity that part of th
23、e connector assembly attached to the pulse generator Note 1 to entry: See Figure 3. 3.4 sealing ring circumferential barrier intended to maintain the electrical insulation between electrically isolated parts of the connector assembly when implanted 3.5 seal zone surface in the connector cavity on wh
24、ich one or more sealing rings on the lead connector are intended to bear 3.6 connector cavity GO gauge tool for assessing the ability of a connector cavity to accept a lead connector of maximum size Note 1 to entry: See Figure 5. 3.7 lead connector GO gauge tool for assessing the ability of a lead c
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