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The global market size of AI based SaMD for medical image in 2023 will be anticipated to reach around 620 billion won (518 million dollars). In order for Korean manufacturers to efficiently obtain CE marking for marketing in the EU countries, the paper is to introduce the recommendation and suggestion of how to reclassify SaMD based on classification rules of MDR because, after introducing the Regulation EU 2017/745, classification rules are quite modified and newly added compared to the Directive 93/42/EEC. In addition, the paper is to provide several rules of MDR that may be applicable to decide the classification of SaMD. Lastly, the paper is to examine and demonstrate various secondary data supported by qualitative data because the paper focuses on the suggestion and recommen- dation with a public trust on the basis of various secondary data conducted by the analysis of field data. In conclusion, the paper found that the previous classification of SaMD followed by the rule of MDD should be reclassified based on the Regulation EU 2017/745. Therefore, the suggestion and recommendation are useful for Korean manufacturers to comprehend the classification of SaMD for marketing in the EU countries.
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참고문헌 (13)
참고문헌 신청
Rep. 2020 New Development Medical Device Forecast Analysis Report
BIS Research / Publication. Global Artificial Intelligence Market in Healthcare Sector: Analysis & Forecasts, 2017-2025 (Focus on Real-Time Monitoring, Precision Medicine, Personal Health & Nursing Assistants and Robot-Assisted Surgery)
BMI Research / Rep. Worldwide Medical Device Market Forecasts to 2021
European Commission / Medical Device Regulation (MDR). Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC
Commission, E. / MDCG 2019-11 Guidance on Qualification and Classification of Software in Regulation (EU)2017/745 – MDR and Regulation (EU) 2017/746 – IVDR. [ebook]
BIS Research / Publication. Global Artificial Intelligence Market in Healthcare Sector: Analysis & Forecasts, 2017-2025 (Focus on Real-Time Monitoring, Precision Medicine, Personal Health & Nursing Assistants and Robot-Assisted Surgery)
BMI Research / Rep. Worldwide Medical Device Market Forecasts to 2021
European Commission / Medical Device Regulation (MDR). Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC
Commission, E. / MDCG 2019-11 Guidance on Qualification and Classification of Software in Regulation (EU)2017/745 – MDR and Regulation (EU) 2017/746 – IVDR. [ebook]
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