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ANSI TIR62354-2009 General testing procedures for medical electrical equipment.pdf

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

25、 wire .188 Annex O (informative) Guideline for safe laboratory work .193 Bibliography 200 Index of defined terms .202 Figure 1 Area of the bottom of an ENCLOSURE as specified in 11.3 b) 1) .30 Figure 2 Baffle30 Figure 3 CREEPAGE DISTANCE and AIR CLEARANCE Example 1 .45 Figure 4 CREEPAGE DISTANCE and

26、 AIR CLEARANCE Example 2 .45 Figure 5 CREEPAGE DISTANCE and AIR CLEARANCE Example 3 .45 Figure 6 CREEPAGE DISTANCE and AIR CLEARANCE Example 4 .46 Figure 7 CREEPAGE DISTANCE and AIR CLEARANCE Example 5 .46 Figure 8 CREEPAGE DISTANCE and AIR CLEARANCE Example 6 .46 Figure 9 CREEPAGE DISTANCE and AIR

27、CLEARANCE Example 7 .47 Figure 10 CREEPAGE DISTANCE and AIR CLEARANCE Example 8 .47 Figure 11 CREEPAGE DISTANCE and AIR CLEARANCE Example 9 .48 Figure 12 Human body test mass66 Figure 13 Application of test voltage to bridged PATIENT CONNECTIONS for DEFIBRILLATION-PROOF APPLIED PARTS .93 Figure 14 A

28、pplication of test voltage to individual PATIENT CONNECTIONS for DEFIBRILLATION-PROOF APPLIED PARTS94 Figure 15 Application of test voltage to test the delivered defibrillation energy .97 Figure 16 Example of a measuring device and its frequency characteristics .99 Figure 17 Measuring circuit for th

29、e EARTH LEAKAGE CURRENT of CLASS I equipment, with or without APPLIED PARTS101 Figure 18 Measuring circuit for the TOUCH CURRENT .104 Figure 19 Measuring circuit for the PATIENT LEAKAGE CURRENT from the PATIENT CONNECTION to earth. .106 Figure 20 Measuring circuit for the total PATIENT LEAKAGE CURRE

30、NT with all PATIENT CONNECTIONS of all APPLIED PARTS of the same type (TYPE B APPLIED PARTS, TYPE BF APPLIED PARTS or TYPE CF APPLIED PARTS) connected together .107 Figure 21 Measuring circuit for the PATIENT LEAKAGE CURRENT via the PATIENT CONNECTION(S) of an F-TYPE APPLIED PART to earth caused by

31、an external voltage on the PATIENT CONNECTION(S) 109 Figure 22 Measuring circuit for the PATIENT LEAKAGE CURRENT from PATIENT CONNECTION(S) to earth caused by an external voltage on a metal ACCESSIBLE PART that is not PROTECTIVELY EARTHED.110 Figure 23 Measuring circuit for the PATIENT LEAKAGE CURRE

32、NT from PATIENT CONNECTION(S) to earth caused by an external voltage on a SIGNAL INPUT/OUTPUT PART112 Figure 24 Measuring circuit for the PATIENT AUXILIARY CURRENT 114 Figure 25 Ratio between HYDRAULIC TEST PRESSURE AND MAXIMUM PERMISSIBLE WORKING PRESSURE 118 Figure 26 Spark ignition test apparatus

33、 .125 Figure 27 Maximum allowable current I as a function of the maximum allowable voltage U measured in a purely resistive circuit in an OXYGEN RICH ENVIRONMENT.127 Figure 28 Maximum allowable voltage U as a function of the capacitance C measured in a capacitive circuit used in an OXYGEN RICH ENVIR

34、ONMENT .127 Figure 29 Maximum allowable current I as a function of the inductance L measured in an inductive circuit in an OXYGEN RICH ENVIRONMENT .128 Figure D.1 Measuring supply circuit with one side of the SUPPLY MAINS at approximately earth potential .159 Figure D.2 Measuring supply circuit with

35、 SUPPLY MAINS approximately symmetrical to earth potential .159 Figure D.3 Measuring supply circuit for polyphase ME EQUIPMENT specified for connection to a polyphase SUPPLY MAINS 160 Figure D.4 Measuring supply circuit for single-phase ME EQUIPMENT specified for connection to a polyphase SUPPLY MAI

36、NS 160 Figure D.5 Measuring supply circuit for ME EQUIPMENT having a separate power supply unit or intended to receive its power from another equipment in an ME SYSTEM 161 Figure F.1 Standard test finger .164 Figure F.2 Test hook 165 Figure F.3 Test pin .165 Figure F.4 Ball-pressure test apparatus.1

37、66 Figure N.1 Thermocouple preparation .188 Figure N.2 Securing of thermocouples.190 Figure N.3 Example of confinement of a thermocouple 190 Figure N.4 Example where thermocouple connectors need not be used .191 Table 1 Units outside the SI units system that may be used.11 Table 2 Tests to be perfor

38、med by inspection .12 Table 3 NOMINAL cross-sectional area of conductors of a POWER SUPPLY CORD23 Table 4 Acceptable perforation of the bottom of an ENCLOSURE 31 Table 5 Measurements and tests performed on non-energized equipment34 Table 6 Testing of cord anchorages 49 Table 7 Acceptable gapsa.55 Ta

39、ble 8 Drop height 80 Table 9 Test torques for rotating controls 86 Table 10 Measurements and tests for equipment that is operating .87 Table 11 Allowable maximum temperatures for skin contact with ME EQUIPMENT APPLIED PARTS135 Table 12 Allowable maximum temperatures for ME EQUIPMENT parts that are l

40、ikely to be touched.135 Table 13 Allowable maximum temperatures of parts 136 Table 14 Temperature limits of motor windings136 Table 15 Maximum motor winding steady-state temperature 137 Table 16 Maximum allowable temperatures of transformer windings under overload and short-circuit conditions at 25

41、C ( 5 C) ambient temperature137 Table 17 Test current for transformers 149 Table C.1 IEC 60601-1:1988 + Amendment 1:1991 and Amendment 2:1995 158 Table D.1 Legends of symbols for Figures D.1 to D.5 162 Table L.1 Method for testing a single phase laboratory power source.183 Glossary of equivalent sta

42、ndards International Standards adopted in the United States may include normative references to other International Standards. For each International Standard that has been adopted by AAMI (and ANSI), the table below gives the corresponding U.S. designation and level of equivalency to the Internatio

43、nal Standard. NOTE: Documents are sorted by international designation. Other normatively referenced International Standards may be under consideration for U.S. adoption by AAMI; therefore, this list should not be considered exhaustive. International designation U.S. designation Equivalency IEC 60601

44、-1:2005 Technical Corrigendum 1 and 2 ANSI/AAMI ES60601-1:2005 ANSI/AAMI ES60601-1:2005/C1:2009 (amdt) Major technical variations C1 Identical to Corrigendum 1 any IEC National Committee interested in the subject dealt with may participate in this preparatory work. International, governmental and no

45、n-governmental organizations liaising with the IEC also participate in this preparation. IEC collaborates closely with the International Organization for Standardization (ISO) in accordance with conditions determined by agreement between the two organizations. 2) The formal decisions or agreements o

46、f IEC on technical matters express, as nearly as possible, an international consensus of opinion on the relevant subjects since each technical committee has representation from all interested IEC National Committees. 3) IEC Publications have the form of recommendations for international use and are

47、accepted by IEC National Committees in that sense. While all reasonable efforts are made to ensure that the technical content of IEC Publications is accurate, IEC cannot be held responsible for the way in which they are used or for any misinterpretation by any end user. 4) In order to promote intern

48、ational uniformity, IEC National Committees undertake to apply IEC Publications transparently to the maximum extent possible in their national and regional publications. Any divergence between any IEC Publication and the corresponding national or regional publication shall be clearly indicated in th

49、e latter. 5) IEC itself does not provide any attestation of conformity. Independent certification bodies provide conformity assessment services and, in some areas, access to IEC marks of conformity. IEC is not responsible for any services carried out by independent certification bodies. 6) All users should ensure that they have the latest edition of this publication. 7) No liability shall attach to IEC or its directors, employees, se

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