Registration number (WIID)Project No.TitleStatus
51298EN 60601-2-33:2010/A2:2015Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosisStandarts spēkā
74642EN IEC 80601-2-77:2021/A1:2023Medical electrical equipment - Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipmentStandarts spēkā
73951LVS EN IEC 60601-2-83:2020/A1:2025Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipmentStandarts spēkā
61909EN IEC 80601-2-60:2020Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipmentStandarts spēkā
54121EN 62304:2006Medical device software - Software life-cycle processesStandarts spēkā
73348LVS EN IEC 63322:2025Security of ME equipment containing high-activity sealed radioactive sourcesStandarts spēkā
55550EN 60601-2-68:2015Medical electrical equipment - Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipmentStandarts spēkā
73951EN IEC 60601-2-83:2020/A1:2025Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipmentStandarts spēkā
50334EN 62570:2015Standard practice for marking medical devices and other items for safety in the magnetic resonance environmentStandarts spēkā
74041EN IEC 60601-2-2:2018/A1:2024Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessoriesStandarts spēkā
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