집속형 초음파 자극 시스템의 사용적합성 형성평가에 대한 연구 및 고찰

Medical device usability evaluation refers to the evaluation of medical devices through actual users before the final prototype production is completed. IEC 62366, one of the international safety standards for electronic medical devices, is a standard that must be applied to obtain medical device li...

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Published in한국정보전자통신기술학회 논문지 Vol. 15; no. 2; pp. 164 - 177
Main Authors 김준태(Jun-tae Kim), 김주희(Ju-hee Kim), 주규태(Kyu-tai Joo), 김경아(Kyung-ah Kim), 류옥수(Ok-su Ryu), 조재현(Jae-hyun Jo), 정진형(Jin-Hyoung Jeong)
Format Journal Article
LanguageKorean
Published 한국정보전자통신기술학회 2022
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ISSN2005-081X
2288-9302

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Abstract Medical device usability evaluation refers to the evaluation of medical devices through actual users before the final prototype production is completed. IEC 62366, one of the international safety standards for electronic medical devices, is a standard that must be applied to obtain medical device licenses in major advanced countries such as Europe and the United States. In Korea, through the Ministry of Food and Drug Safety's notice, from January 2021, sequential application by grade has been implemented. In this study, 15 participant specialists were recruited through the Incheon G University Hospital Medical Device Convergence Center for formative evaluation during user suitability evaluation of the focused ultrasound stimulation system being developed by Icleo Co., Ltd., and the test was conducted through joint scenario development. . In the result of task performance, the performance rate was 90.67%, and after the completion of the performance, 86.67% of 'Easy user interface' and 94% of 'Identification/Readability/Understanding of information' questions in the participant survey results analysis by question. The response rate was above average. 의료기기 사용적합성 평가란 최종 시제품 제작 완료이전 실제 사용자를 통한 의료기기의 평가를 말한다. 국제전자의료기기 안전규격 중 하나인 IEC 62366은 유럽 및 미국 등 주요 선진국의 의료기기 인허가 획득을 위해 반드시 적용해야 하는 규격이다. 국내의 경우 식약처 고시를 통하여 2021년 1월부터 등급별로 순차적 적용을 시행하고 있다. 본 연구에서는 (주)이끌레오에서 개발 중인 집중형초음파자극시스템의 사용자 적합성 평가 중 형성평가를 인천 G 대학 병원 의료기기융합 센터를 통하여 참가자 전문의 15인을 모집하였고, 공동 시나리오 개발을 통하여 시험을 진행하였다. 작업 수행 여부 결과에서는 90.67%의 수행율을 보였으며, 수행 완료 후 참가자 설문 조사결과 문항별 결과 분석에서 '사용자 인터페이스의 용이성' 86.67%, '정보의 식별성/가독성/이해도' 문항에서 94%의 보통 이상의 응답 비율을 보였다.
AbstractList 의료기기 사용적합성 평가란 최종 시제품 제작 완료이전 실제 사용자를 통한 의료기기의 평가를 말한다. 국제 전자의료기기 안전규격 중 하나인 IEC 62366은 유럽 및 미국 등 주요 선진국의 의료기기 인허가 획득을 위해 반드시 적용해야 하는 규격이다. 국내의 경우 식약처 고시를 통하여 2021년 1월부터 등급별로 순차적 적용을 시행하고 있다. 본 연구에서는 ㈜이끌레오에서 개발 중인 집중형초음파자극시스템의 사용자 적합성 평가 중 형성평가를 인천 G 대학 병원 의료기기융합 센터를 통하여 참가자 전문의 15인을 모집하였고, 공동 시나리오 개발을 통하여 시험을 진행하였다. 작업 수행 여부 결과에서는 90.67%의 수행율을 보였으며, 수행 완료 후 참가자 설문 조사결과 문항별 결과 분석에서 ‘사용자 인터페이스의 용이성’ 86.67%, ‘정보의 식별성/가독성/이해도’ 문항에서 94%의 보통 이상의 응답 비율을 보였다. Medical device usability evaluation refers to the evaluation of medical devices through actual users before the final prototype production is completed. IEC 62366, one of the international safety standards for electronic medical devices, is a standard that must be applied to obtain medical device licenses in major advanced countries such as Europe and the United States. In Korea, through the Ministry of Food and Drug Safety's notice, from January 2021, sequential application by grade has been implemented. In this study, 15 participant specialists were recruited through the Incheon G University Hospital Medical Device Convergence Center for formative evaluation during user suitability evaluation of the focused ultrasound stimulation system being developed by Icleo Co., Ltd., and the test was conducted through joint scenario development. . In the result of task performance, the performance rate was 90.67%, and after the completion of the performance, 86.67% of 'Easy user interface' and 94% of 'Identification/Readability/Understanding of information' questions in the participant survey results analysis by question. The response rate was above average. KCI Citation Count: 0
Medical device usability evaluation refers to the evaluation of medical devices through actual users before the final prototype production is completed. IEC 62366, one of the international safety standards for electronic medical devices, is a standard that must be applied to obtain medical device licenses in major advanced countries such as Europe and the United States. In Korea, through the Ministry of Food and Drug Safety's notice, from January 2021, sequential application by grade has been implemented. In this study, 15 participant specialists were recruited through the Incheon G University Hospital Medical Device Convergence Center for formative evaluation during user suitability evaluation of the focused ultrasound stimulation system being developed by Icleo Co., Ltd., and the test was conducted through joint scenario development. . In the result of task performance, the performance rate was 90.67%, and after the completion of the performance, 86.67% of 'Easy user interface' and 94% of 'Identification/Readability/Understanding of information' questions in the participant survey results analysis by question. The response rate was above average. 의료기기 사용적합성 평가란 최종 시제품 제작 완료이전 실제 사용자를 통한 의료기기의 평가를 말한다. 국제전자의료기기 안전규격 중 하나인 IEC 62366은 유럽 및 미국 등 주요 선진국의 의료기기 인허가 획득을 위해 반드시 적용해야 하는 규격이다. 국내의 경우 식약처 고시를 통하여 2021년 1월부터 등급별로 순차적 적용을 시행하고 있다. 본 연구에서는 (주)이끌레오에서 개발 중인 집중형초음파자극시스템의 사용자 적합성 평가 중 형성평가를 인천 G 대학 병원 의료기기융합 센터를 통하여 참가자 전문의 15인을 모집하였고, 공동 시나리오 개발을 통하여 시험을 진행하였다. 작업 수행 여부 결과에서는 90.67%의 수행율을 보였으며, 수행 완료 후 참가자 설문 조사결과 문항별 결과 분석에서 '사용자 인터페이스의 용이성' 86.67%, '정보의 식별성/가독성/이해도' 문항에서 94%의 보통 이상의 응답 비율을 보였다.
Author 류옥수(Ok-su Ryu)
정진형(Jin-Hyoung Jeong)
주규태(Kyu-tai Joo)
조재현(Jae-hyun Jo)
김주희(Ju-hee Kim)
김준태(Jun-tae Kim)
김경아(Kyung-ah Kim)
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DocumentTitleAlternate Research and consideration on the evaluation of usability formation of focused ultrasonic stimulation systems
DocumentTitle_FL Research and consideration on the evaluation of usability formation of focused ultrasonic stimulation systems
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Snippet Medical device usability evaluation refers to the evaluation of medical devices through actual users before the final prototype production is completed. IEC...
의료기기 사용적합성 평가란 최종 시제품 제작 완료이전 실제 사용자를 통한 의료기기의 평가를 말한다. 국제 전자의료기기 안전규격 중 하나인 IEC 62366은 유럽 및 미국 등 주요 선진국의 의료기기 인허가 획득을 위해 반드시 적용해야 하는 규격이다. 국내의 경우 식약처 고시를 통하여...
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SubjectTerms 전자/정보통신공학
Title 집속형 초음파 자극 시스템의 사용적합성 형성평가에 대한 연구 및 고찰
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