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Analysis of Medical Device Class Changes Caused when European Regulation (MDR) is Applied to Classes of Korean Software as a Medical Device (SaMD) Items

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  • 발행기관
    한국에프디시규제과학회(구 한국에프디시법제학회) 바로가기
  • 간행물
    KFDC규제과학회지(구 FDC법제연구) 바로가기
  • 통권
    17권 1호 (2022.06)바로가기
  • 페이지
    pp.79-85
  • 저자
    Lee ji yoon, Ryu gyu ha
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A415644

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초록

영어
At present, the domestic and overseas markets for artificial intelligence (AI)-based Software as a Medical Device (SaMD) services for medical video are rapidly increasing. Moreover, the future is also promising. In South Korea, AI-based software (SW) utilizing video and medical big data accounts for a large proportion of Korean SaMD standard diagnosis/detection assistance SaMD SW approved by Ministry of Food and Drug Safety (MFDS) and used for clinical experiments. Future work will focus on device development. Furthermore, Europe is currently the world’s second-largest market for medical devices. As a result, Korean manufacturers may explore marketing medical products to EU countries. However, the Korean medical device classification system and the European medical device classification system are different. In addition, European regulation is in flux, with an old standard (MDD) currently being updated to a new one (MDR); this presents additional factors that SaMD producers should consider. This paper presents the medical device grades that should be considered first for export. In addition, this paper also explains which provisions applicable to SaMD exist in MDR, as well as how Korean medical device (i.e., Korean SaMD standard diagnostic and detection assistance software) grades will change according to the new European legal standard (MDR).

목차

Abstract
I. Introduction
II. Analysis of Medical Device
1. Korean medical device classification system
2. SaMD classification by item in South Korea
3. The European MDSW classification system
4. SaMD of MDR: classification of SaMD: Implementing Rules
5. MDR classification of SaMDs: Classification Rules
III. Re-classification of Korean SaMD according the MDR classification
1. Endoscopic imaging and computer-aided detection/diagnosis software, Class 2: Class IIa
2. Ultrasound imaging and computer-aided detection/diagnosis software, Class 2: Class IIa
3. Breast cancer image, computer aided detection/diagnosis software, Class 3: Class IIb
4. Gastric cancer imaging and computer-aided detection/diagnosis software: Class IIb
5. Prostate cancer imaging and computer-aided detection/diagnosis software: Class IIb
6. Ultrasound imaging and computer-aided detection/diagnosis software, Class 3: Class IIb
IV. Conclusion
References

키워드

SaMD (Software as a Medical Device) MDSW (Medical Device Software) MDD (Medical Device Directive Directive 93/42/EEC) MDR (Medical Device regulation Regulation EU 2017/745)

저자

  • Lee ji yoon [ Dipartment of Medical Device Management and Research, SAIHST, Sungkyunkwan University, Seoul 06351, Korea ]
  • Ryu gyu ha [ Dipartment of Medical Device Management and Research, SAIHST, Sungkyunkwan University, Seoul 06351, Korea ] Corresponding Author

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국에프디시규제과학회(구 한국에프디시법제학회) [The Korean Society of Food, Drug and Cosmetic Regulatory Sciences]
  • 설립연도
    2006
  • 분야
    의약학>약학
  • 소개
    본회는 의약품, 의약외품, 의료기기, 화장품 및 건강기능식품 등과 관련된 국내·외의 각종 법령과 규정 등에 대한 연구와 발표 등을 통하여 합리적이고 투명한 법령과 규정의 제·개정 및 정책개발에 기여함으로써 관련 산업의 발전과 국민의 건강증진에 기여하며 회원 상호 간의 친목을 도모함을 목적으로 한다.

간행물

  • 간행물명
    KFDC규제과학회지(구 FDC법제연구) [Regulatory Research on Food, Drug and Cosmetic]
  • 간기
    반년간
  • pISSN
    2799-8940
  • 수록기간
    2006~2025
  • 십진분류
    KDC 518 DDC 615

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