ANSI TIR62354-2009 General testing procedures for medical electrical equipment.pdf
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1、ANSI/AAMI/IEC TIR62354:2009 Association for the Advancementof Medical InstrumentationGeneral testing procedures for medical electrical equipmentAn ANSI Technical Report prepared by AAMI ANSI/AAMI/IEC TIR62354:2009 General testing procedures for medical electrical equipment Approved 31 December 2009
2、by Association for the Advancement of Medical Instrumentation Registered 21 February 2010 by American National Standards Institute, Inc. Abstract: This Technical Report specifies the general harmonized recommendations (conditions and procedures) for testing MEDICAL ELECTRICAL EQUIPMENT (as defined i
3、n Sub-clause 2.2.15 of IEC 60601-1, 2nd edition). This Technical Report is primarily intended to be used by test houses and others responsible for assessment of compliance with IEC 60601-1. Keywords: medical electrical equipment, assessment, testing, maintenance, electrical safety Published by Assoc
4、iation for the Advancement of Medical Instrumentation 1110 N. Glebe Rd., Suite 220 Arlington, VA 22201-4795 www.aami.org 2010 by the Association for the Advancement of Medical Instrumentation All Rights Reserved This publication is subject to copyright claims of ISO, ANSI, and AAMI. No part of this
5、publication may be reproduced or distributed in any form, including an electronic retrieval system, without the prior written permission of AAMI. All requests pertaining to this draft should be submitted to AAMI. It is illegal under federal law (17 U.S.C. 101, et seq.) to make copies of all or any p
6、art of this document (whether internally or externally) without the prior written permission of the Association for the Advancement of Medical Instrumentation. Violators risk legal action, including civil and criminal penalties, and damages of $100,000 per offense. For permission regarding the use o
7、f all or any part of this document, complete the reprint request form at www.aami.org or contact AAMI, 1110 N. Glebe Road, Suite 220, Arlington, VA 22201-4795. Phone: (703) 525-4890; Fax: (703) 525-1067. Printed in the United States of America ISBN 1570203776 AAMI Technical Information Report A tech
8、nical information report (TIR) is a publication of the Association for the Advancement of Medical Instrumentation (AAMI) Standards Board that addresses a particular aspect of medical technology. Although the material presented in a TIR might need further evaluation by experts, releasing the informat
9、ion is valuable because the industry and the professions have an immediate need for it. A TIR differs markedly from a standard or recommended practice, and readers should understand the differences between these documents. Standards and recommended practices are subject to a formal process of commit
10、tee approval, public review, and resolution of all comments. This process of consensus is supervised by the AAMI Standards Board and, in the case of American National Standards, by the American National Standards Institute. A TIR is not subject to the same formal approval process as a standard. Howe
11、ver, a TIR is approved for distribution by a technical committee and the AAMI Standards Board. Another difference is that, although both standards and TIRs are periodically reviewed, a standard must be acted onreaffirmed, revised, or withdrawnand the action formally approved usually every five years
12、 but at least every 10 years. For a TIR, AAMI consults with a technical committee about five years after the publication date (and periodically thereafter) for guidance on whether the document is still usefulthat is, to check that the information is relevant or of historical value. If the informatio
13、n is not useful, the TIR is removed from circulation. A TIR may be developed because it is more responsive to underlying safety or performance issues than a standard or recommended practice or because achieving consensus is extremely difficult or unlikely. Unlike a standard, a TIR permits the inclus
14、ion of differing viewpoints on technical issues. CAUTION NOTICE: This AAMI TIR may be revised or withdrawn at any time. Because it addresses a rapidly evolving field or technology, readers are cautioned to ensure that they have also considered information that might be more recent than this document
15、. All standards, recommended practices, technical information reports, and other types of technical documents developed by AAMI are voluntary, and their application is solely within the discretion and professional judgment of the user of the document. Occasionally, voluntary technical documents are
16、adopted by government regulatory agencies or procurement authorities, in which case the adopting agency is responsible for enforcement of its rules and regulations. Comments on this technical information report are invited and should be sent to AAMI, Attn: Standards Department, 1110 N. Glebe Road, S
17、uite 220, Arlington, VA 22201-4795. ANSI Technical Report This AAMI TIR has been registered by the American National Standards Institute as an ANSI Technical Report. Publication of this ANSI Technical Report has been approved by the accredited standards developer (AAMI). This document is registered
18、as a Technical Report series of publications according to the Procedures for the Registration of Technical Reports with ANSI. This document is not an American National Standard and the material contained herein is not normative in nature. Comments on the content of this document should be sent to AA
19、MI, Attn: Standards Department, 1110 N. Glebe Road, Suite 220, Arlington, VA 22201-4795. Contents Page Glossary of equivalent standards viii Committee representation . x Background of ANSI/AAMI adoption of IEC/TR 62354:2009 xi FOREWORD . xii INTRODUCTION xiv 1 Scope and object . 1 2 Normative refere
20、nces . 1 3 Terms, definitions, abbreviations and acronyms 2 4 Types of tests 3 5 State of the ME EQUIPMENT 4 6 Number of samples 4 7 Applicable test items to the clauses of IEC 60601-1 4 8 Sequence of tests 4 9 General testing condition 5 10 Power sources for tests 6 11 Measurement and test equipmen
21、t . 8 12 Treatments of unit symbols and measured values 10 13 PROCEDURES for testing, including particular conditions11 Annex A (informative) Sequence of testing153 Annex B (informative) Information typically required for product safety testing (Guide).156 Annex C (informative) Testing and measuring
22、 equipment 158 Annex D (informative) Suitable measuring supply circuits 159 Annex E (informative) Preventive maintenance .163 Annex F (informative) Test probes 164 Annex G (informative) Index of tests (IEC 60601-1:2005 clauses order).167 Annex H (informative) Index of tests for an INTERNALLY POWERED
23、 EQUIPMENT battery only (IEC 60601-1:2005 clauses order)170 Annex I (informative) Index of tests (IEC 60601-1:2005 alphabetic order) 172 Annex J (informative) Index of tests for an INTERNALLY POWERED EQUIPMENT battery only (IEC 60601-1:2005 alphabetic order)175 Annex K (informative) Production line
24、tests .177 Annex L (informative) Evaluation of the laboratory power source characteristics .181 Annex M (informative) Traceability of calibrations and calibration intervals .186 Annex N (informative) Guidance for preparation, attachment, extension, use of thermocouples and acceptance of thermocouple
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