dc.creator | Pedroso J.C.L. | |
dc.creator | Calil S.J. | |
dc.date | 2009 | |
dc.date | 2015-06-26T13:32:55Z | |
dc.date | 2015-11-26T15:30:35Z | |
dc.date | 2015-06-26T13:32:55Z | |
dc.date | 2015-11-26T15:30:35Z | |
dc.date.accessioned | 2018-03-28T22:39:03Z | |
dc.date.available | 2018-03-28T22:39:03Z | |
dc.identifier | 9783642038846 | |
dc.identifier | Ifmbe Proceedings. , v. 25, n. 7, p. 699 - 702, 2009. | |
dc.identifier | 16800737 | |
dc.identifier | 10.1007/978-3-642-03885-3-194 | |
dc.identifier | http://www.scopus.com/inward/record.url?eid=2-s2.0-77949808359&partnerID=40&md5=3392a0d57cb221cce982d75ca738d69b | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/91636 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/91636 | |
dc.identifier | 2-s2.0-77949808359 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1262024 | |
dc.description | This paper presents a comprehensive framework for electrical safety testing and performance assessment of medical equipment, to be conducted as routine tests in health care facilities by clinical engineering personnel. The rationale for it is that very little has been published in terms of protocols, guidelines, policies and/or technical standards for post market evaluation of medical equipment. Whilst type tests prescribed by current technical standards ultimately aim at ensuring minimally optimal safety and performance conditions for marketing medical devices, the lack of a harmonized framework for post-market routine testing combined with the fact that medical electrical equipment, especially in the developing and least developed world, is subject to sub-optimal conditions of electrical power systems, equipment maintenance and user education, altogether can compromise patient safety. A methodology consistently elaborated and implemented, thoroughly validated by clinical engineering personnel, making use of commercially available analyzers and simulators, yielded the proposed framework. © 2009 Springer-Verlag. | |
dc.description | 25 | |
dc.description | 7 | |
dc.description | 699 | |
dc.description | 702 | |
dc.description | Langanke Pedroso, J.C., Ferreira Filho, J.A., Desenvolvimento de um Programa de Seguranca Eletrica e Avaliacao de Desempenho para Equipamentos Eletromedicos Baseado nas Normas da Familia NBRIEC60601. CBEB2000 Proc. (2000) Congresso Brasileiro de Engenharia Biomedica, 17. , Florianopolis, Brazil | |
dc.description | (2005) IEC60601-1: Medical electrical equipment - Part 1: General requirements for basic safety and essential performance, , International Electrotechnical Commission, Third edition. IEC | |
dc.description | (2007) IEC62353: Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment, , International Electrotechnical Commission, First edition. IEC | |
dc.description | (2008) IEC/TR60930: Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment, , International Electrotechnical Commission, Second edition. IEC | |
dc.description | Langanke Pedroso, J.C., Calil, S.J., Electrical Safety And Performance Assessment Program For Medical Electrical Equipment, Based Upon The NBRIEC60601 Standards And ECRI's IPM System (2003) IFMBE Proc. World Congress on Med. Phys. & Biomed. Eng, , Sydney, Australia | |
dc.description | International Electrotechnical Commission. IEC60601-2-25: Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs. First edition. IEC,1993(2005) IEC60601-2-27: Medical electrical equipment - Part 2-27: Particular requirements for the safety, including essential performance, of electrocardiographic monitoring equipment, , International Electrotechnical Commission, Second edition. IEC | |
dc.description | (2002) IEC60601-2-4: Medical electrical equipment - Part 2-4: Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac defibrillators, , International Electrotechnical Commission, Second edition. IEC | |
dc.description | International Electrotechnical Commission. IEC60601-2-24: Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers. First edition. IEC,1998(2009) IEC60601-2-2: Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories, , International Electrotechnical Commission, Fifth edition. IEC | |
dc.description | (2001) IEC60601-2-12: Medical electrical equipment - Part 2-12: Particular requirements for the safety of lung ventilators - Critical care ventilators, , International Electrotechnical Commission, Second edition. IEC | |
dc.description | (2003) IEC60601-2-13: Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems, , International Electrotechnical Commission, Third edition. IEC | |
dc.description | International Electrotechnical Commission. IEC/TR3 61288-2: Technical report - Cardiac defibrillators - Cardiac defibrillator-monitors - Part 2: Maintenance. First edition. IEC, 1993(1994) IEC/TR3 61289-2: Technical report - High frequency surgical equipment - Part 2, , International Electrotechnical Commission, Maintenance. First edition. IEC | |
dc.description | Health Devices Inspection and Preventive Maintenance System. Third Edition. The Emergency Care Research Institute. Plymouth Meeting, PA, USA: ECRI, 1995. ISBN 0-941417-41-7 | |
dc.language | en | |
dc.publisher | | |
dc.relation | IFMBE Proceedings | |
dc.rights | fechado | |
dc.source | Scopus | |
dc.title | A Comprehensive Framework For Post-market Electrical Safety Testing And Performance Assessment Of Medical Equipment In Healthcare Facilities | |
dc.type | Actas de congresos | |