ANSI TIR10993-19-2006 Biological evaluation of medical devices - Part 19 Physico-chemical morphological and topographical characterization of materials.pdf

《ANSI TIR10993-19-2006 Biological evaluation of medical devices - Part 19 Physico-chemical morphological and topographical characterization of materials.pdf》由会员分享，可在线阅读，更多相关《ANSI TIR10993-19-2006 Biological evaluation of medical devices - Part 19 Physico-chemical morphological and topographical characterization of materials.pdf（29页珍藏版）》请在麦多课文档分享上搜索。

1、ANSI/AAMI/ISO TIR10993-19:2006Biological evaluation of medicaldevices Part 19: Physico-chemical, morphological, andtopographical characterizationof materialsTechnicalInformationReportAssociation for the Advancementof Medical InstrumentationAn ANSI Technical Report prepared by AAMI ANSI/AAMI/ISO TIR1

2、0993-19:2006 Biological evaluation of medical devices Part 19: Physico-chemical, morphological, and topographical characterization of materials Approved 17 October 2005 by Association for the Advancement of Medical Instrumentation Registered 20 November 2005 by American National Standards Institute

3、Abstract: Provides a compilation of parameters and test methods that can be useful for the identification and evaluation of the physico-chemical, morphological, and topographical (PMT) properties of materials in finished medical devices. Keywords: physico-chemical, morphological, topographical Copyr

4、ight information Published by Association for the Advancement of Medical Instrumentation 1110 N. Glebe Road, Suite 220 Arlington, VA 22201-4795 2006 by the Association for the Advancement of Medical Instrumentation All Rights Reserved This publication is subject to copyright claims of ISO, ANSI, and

5、 AAMI. No part of this 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

6、 copies of all or any part 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 permiss

7、ion regarding the use of all or any part of this document, 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 1570202664 AAMI Technical Information Report A technical information report (TIR)

8、 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 may need further evaluation by experts, releasing the information is valuable because the indu

9、stry 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 committee approval, public review, and

10、 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. However, a TIR is approved for distr

11、ibution 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 but at least every 10 years. Fo

12、r 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 information is not useful, the TIR is remo

13、ved 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 inclusion of differing viewpoints on

14、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 may be more recent than this document. All standards, recommended prac

15、tices, 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 adopted by government regulatory

16、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, Suite 220, Arlington, VA 22201-479

17、5. 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 as a Technical Report series of p

18、ublications according to the Procedures for the Registration of ANSI Technical Reports. This document is not an American National Standard and the material contained herein is not normative in nature. Contents Page Glossary of equivalent standards v Committee representation. vii Background of AAMI a

19、doption of ISO/TS 10993-19:2006 .ix Foreword. x Introduction xii 1 Scope 1 2 Normative references . 1 3 Terms and definitions. 1 4 Symbols and abbreviated terms 2 5 General principles. 3 6 Characterization procedure . 4 6.1 General. 4 6.2 Qualitative information. 4 6.3 Material equivalence. 4 6.4 Qu

20、antitative information. 5 6.5 Quantitative assessment 5 7 Characterization parameters and methods 5 8 Reporting of data obtained 9 Annex A (informative) Principles for judging material equivalency. 10 Annex B (informative) Nanoparticles Special consideration in judging material equivalency and biolo

21、gical evaluation . 11 Bibliography . 12 2006 Association for the Advancement of Medical Instrumentation ANSI/AAMI/ISO TIR10993-19:2006 v Glossary of equivalent standards International standards adopted in the United States may include normative references to other international standards. For each i

22、nternational standard that has been adopted by AAMI (and ANSI), the table below gives the corresponding U.S. designation and level of equivalency to the international standard. (Note: Documents are sorted by international designation.) Other normatively referenced international standards may be unde

23、r consideration for U.S. adoption by AAMI; therefore, this list should not be considered exhaustive. International designation U.S. designation Equivalency IEC 60601-1:2005 ANSI/AAMI ES60601-1:2005 Major technical variations IEC 60601-1-2:2001 and Amendment 1:2004 ANSI/AAMI/IEC 60601-1-2:2001 and Am

24、endment 1:2004 Identical IEC 60601-2-04:2002 ANSI/AAMI DF80:2003 Major technical variations IEC 60601-2-19:1990 and Amendment 1:1996 ANSI/AAMI II36:2004 Major technical variations IEC 60601-2-20:1990 and Amendment 1:1996 ANSI/AAMI II51:2004 Major technical variations IEC 60601-2-21:1994 and Amendmen

25、t 1:1996 ANSI/AAMI/IEC 60601-2-21 and Amendment 1:2000 (consolidated texts) Identical IEC 60601-2-24:1998 ANSI/AAMI ID26:2004 Major technical variations IEC/TR 60878:2003 ANSI/AAMI/IEC TIR60878:2003 Identical IEC/TR 62296:2003 ANSI/AAMI/IEC TIR62296:2003 Identical IEC 62304:2006 ANSI/AAMI/IEC 62304:

26、2006 Identical IEC/TR 62348:200x1 ANSI/AAMI/IEC TIR62348:2006 Identical ISO 5840:2005 ANSI/AAMI/ISO 5840:2005 Identical ISO 7198:1998 ANSI/AAMI/ISO 7198:1998/2001/(R)2004 Identical ISO 7199:1996 ANSI/AAMI/ISO 7199:1996/(R)2002 Identical ISO 10993-1:2003 ANSI/AAMI/ISO 10993-1:2003 Identical ISO 10993

27、-2:2006 ANSI/AAMI/ISO 10993-2:200x2Identical ISO 10993-3:2003 ANSI/AAMI/ISO 10993-3:2003 Identical ISO 10993-4:2002 ANSI/AAMI/ISO 10993-4:2002 Identical ISO 10993-5:1999 ANSI/AAMI/ISO 10993-5:1999 Identical ISO 10993-6:1994 ANSI/AAMI/ISO 10993-6:1995/(R)2001 Identical ISO 10993-7:1995 ANSI/AAMI/ISO

28、10993-7:1995/(R)2001 Identical ISO 10993-9:1999 ANSI/AAMI/ISO 10993-9:1999/(R)2005 Identical ISO 10993-10:2002 and Amendment 1:2006 ANSI/AAMI BE78:2002 ANSI/AAMI BE78:2002/A1:2006 Minor technical variations Identical ISO 10993-11:1993 ANSI/AAMI 10993-11:1993 Minor technical variations ISO 10993-12:2

29、002 ANSI/AAMI/ISO 10993-12:2002 Identical ISO 10993-13:1998 ANSI/AAMI/ISO 10993-13:1999/(R)2004 Identical ISO 10993-14:2001 ANSI/AAMI/ISO 10993-14:2001 Identical ISO 10993-15:2000 ANSI/AAMI/ISO 10993-15:2000 Identical ISO 10993-16:1997 ANSI/AAMI/ISO 10993-16:1997/(R)2003 Identical ISO 10993-17:2002

30、ANSI/AAMI/ISO 10993-17:2002 Identical ISO 10993-18:2005 ANSI/AAMI BE83:2006 Major technical variations ISO/TS 10993-19:2006 ANSI/AAMI/ISO TIR10993-19:2006 Identical vi 2006 Association for the Advancement of Medical Instrumentation ANSI/AAMI/ISO TIR10993-19:2006 International designation U.S. design

31、ation Equivalency ISO/TS 10993-20:200x1ANSI/AAMI/ISO TIR10993-20:2006 Identical ISO 11135:1994 ANSI/AAMI/ISO 11135:1994 Identical ISO 11137-1:2006ANSI/AAMI/ISO 11137-1:2006 Identical ISO 11137-2:200x1 ANSI/AAMI/ISO 11137-2:2006 Identical ISO 11137-3:2006ANSI/AAMI/ISO 11137-3:2006 Identical ISO 11138

32、-1: 2006 ANSI/AAMI/ISO 11138-1:2006 Identical ISO 11138-2: 2006 ANSI/AAMI/ISO 11138-2:2006 Identical ISO 11138-3: 2006 ANSI/AAMI/ISO 11138-3:2006 Identical ISO 11138-4: 2006 ANSI/AAMI/ISO 11138-4:2006 Identical ISO 11138-5: 2006 ANSI/AAMI/ISO 11138-5:2006 Identical ISO/TS 11139:2006 ANSI/AAMI/ISO 11

33、139:2006 Identical ISO 11140-1:2005 ANSI/AAMI/ISO 11140-1:2005 Identical ISO 11140-5:2000 ANSI/AAMI ST66:1999 Major technical variations ISO 11607-1:2006ANSI/AAMI/ISO 11607-1:2006 Identical ISO 11607-2:2006ANSI/AAMI/ISO 11607-2:2006 Identical ISO 11737-1: 2006 ANSI/AAMI/ISO 11737-1:2006 Identical IS

34、O 11737-2:1998 ANSI/AAMI/ISO 11737-2:1998 Identical ISO 11737-3:2004 ANSI/AAMI/ISO 11737-3:2004 Identical ISO 13485:2003 ANSI/AAMI/ISO 13485:2003 Identical ISO 13488:1996 ANSI/AAMI/ISO 13488:1996 Identical ISO 14155-1:2003 ANSI/AAMI/ISO 14155-1:2003 Identical ISO 14155-2:2003 ANSI/AAMI/ISO 14155-2:2

35、003 Identical ISO 14160:1998 ANSI/AAMI/ISO 14160:1998 Identical ISO 14161:2000 ANSI/AAMI/ISO 14161:2000 Identical ISO 14937:2000 ANSI/AAMI/ISO 14937:2000 Identical ISO/TR 14969:2004 ANSI/AAMI/ISO TIR14969:2004 Identical ISO 14971:2000 and A1:2003 ANSI/AAMI/ISO 14971:2000 and A1:2003 Identical ISO 15

36、223:2000, A1:2002, and A2:2004 ANSI/AAMI/ISO 15223:2000, A1:2001, and A2:2004 Identical ISO 15225:2000 and A1:2004 ANSI/AAMI/ISO 15225:2000/(R)2006 and A1:2004/(R)2006 Identical ISO 15674:2001 ANSI/AAMI/ISO 15674:2001 Identical ISO 15675:2001 ANSI/AAMI/ISO 15675:2001 Identical ISO/TS 15843:2000 ANSI

37、/AAMI/ISO TIR15843:2000 Identical ISO 15882:2003 ANSI/AAMI/ISO 15882:2003 Identical ISO/TR 16142:2006 ANSI/AAMI/ISO TIR16142:2006 Identical ISO 17664:2004 ANSI/AAMI ST81:2004 Major technical variations ISO 17665-1:200x1ANSI/AAMI/ISO 17665-1:2006 Identical ISO 18472:2006 ANSI/AAMI/ISO 18472:2006 Iden

38、tical ISO/TS 19218:2005 ANSI/AAMI/ISO 19218:2005 Identical ISO 25539-1:2003 and A1:2005 ANSI/AAMI/ISO 25539-1:2003 and A1:2005 Identical 2006 Association for the Advancement of Medical Instrumentation ANSI/AAMI/ISO TIR10993-19:2006 vii Committee representation Association for the Advancement of Medi

39、cal Instrumentation Biological Evaluation of Medical Devices Committee The adoption of ISO Technical Specification (TS) 10993-19:2006 as an AAMI Technical Information Report was initiated by the AAMI Biological Evaluation of Medical Devices Committee, which also functions as a U.S. Technical Advisor

40、y Group to the relevant work in the International Organization for Standardization (ISO). U.S. representatives from the AAMI Material Characterization Working Group (U.S. Sub-TAG for ISO/TC 194/WG 14) played an active part in developing the ISO Technical Specification. At the time this document was

41、published, the AAMI Biological Evaluation of Medical Devices Committee had the following members: Cochairs: Donald E. Marlowe Peter William Urbanski Members: James M. Anderson, MD, PhD, Case Western Reserve University (Independent Expert) Roger Dabbah, PhD, US Pharmacopeia Convention Inc Lawrence H.

42、 Hecker, PhD, Hospira Inc John G. Miller, DVM, AAALAC International Barry F.J. Page, Barry Page Consulting (Independent Expert) Anita Y. Sawyer, Becton Dickinson an ISO Technical Specification (ISO/TS) represents an agreement between the members of a technical committee and is accepted for publicati

43、on if it is approved by 2/3 of the members of the committee casting a vote. An ISO/PAS or ISO/TS is reviewed after three years in order to decide whether it will be confirmed for a further three years, revised to become an International Standard, or withdrawn. If the ISO/PAS or ISO/TS is confirmed,

44、it is reviewed again after a further three years, at which time it must either be transformed into an International Standard or be withdrawn. 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 id

45、entifying any or all such patent rights. ISO/TS 10993-19 was prepared by Technical Committee ISO/TC 194, Biological evaluation of medical devices. ISO 10993 consists of the following parts, under the general title Biological evaluation of medical devices: Part 1: Evaluation and testing Part 2: Anima

46、l welfare requirements Part 3: Tests for genotoxicity, carcinogenicity, and reproductive toxicity Part 4: Selection of tests for interactions with blood Part 5: Tests for in vitro cytotoxicity 2006 Association for the Advancement of Medical Instrumentation ANSI/AAMI/ISO TIR10993-19:2006 xi Part 6: T

47、ests for local effects after implantation Part 7: Ethylene oxide sterilization residuals Part 9: Framework for identification and quantification of potential degradation products Part 10: Tests for irritation and delayed-type hypersensitivity Part 11: Tests for systemic toxicity Part 12: Sample prep

48、aration and reference materials Part 13: Identification and quantification of degradation products from polymeric medical devices Part 14: Identification and quantification of degradation products from ceramics Part 15: Identification and quantification of degradation products from metals and alloys

49、 Part 16: Toxicokinetic study design for degradation products and leachables Part 17: Establishment of allowable limits for leachable substances Part 18: Chemical characterization of materials Part 19: Physico-chemical, morphological, and topographical characterization of materials Part 20: Principles and methods for immunotoxicology testing of medical devices xii 2006 Association for the Advancement of Medical Instrumentation ANSI/AAMI/ISO TIR10993-19:2006 Introd