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        • 04_G11_MEDDEV_2_1_6_072016_en
        • 04_G12_MedDev_2_7_1_rev4_en Clinical Evaluation
        • 04_G13_2023 C 163 06_Summary of the CIR
        • 04_G14_MDGC_Transitional provision under article 120_2020-3_en
        • 04_G15_Manual on borderline and classification for medical devices
        • 04_G16_Principles and Practices for Medical Device Cybersecurity
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  • External documentation
  • 04 EU 🇪🇺 Medical devices
  • Guides
  • 04_G11_MEDDEV_2_1_6_072016_en

04_G11_MEDDEV_2_1_6_072016_en

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