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유럽 |
지침 |
Team-NB-PositionPaper-BPG-TechnicalDocEU-MDR-2017-745-V2.
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2023-12-19 |
| 6 |
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지침 |
[MDCG 2023-3] Questions and Answers on vigilance terms and concepts as outlined in the Regulation (EU) 2017/745 on medical devices
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2023-12-19 |
| 5 |
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[MDCG 2022-14] Transition to the MDR and IVDR - Notified body capacity and availability of medical devices and IVDs
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2023-12-19 |
| 4 |
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[MDCG 2022-13] Designation, re-assessment and notification of conformity assessment bodies and notified bodies
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2023-12-19 |
| 3 |
유럽 |
지침 |
[MDCG 2022-4] Guidance on appropriate surveillance regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD
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2023-12-19 |
| 2 |
유럽 |
지침 |
MDCG 2023-3, Questions and Answers on vigilance terms and concepts as outlined in the Regulation(EU) 2017/745 on medical devices
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2023-11-27 |
| 1 |
유럽 |
소식지 |
[한국의료기기안전정보원] 유럽(CE) 의료기기 MDR 제도 이해 및 대응 전략 보고서
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2023-07-19 |
