CLC/TC 62
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 66675 | LVS EN IEC 80001-1:2022 | Application of risk management for IT-networks incorporating medical devices - Part 1: Safety, effectiveness and security in the implementation and use of connected medical devices or connected health software | Standarts spēkā |
| 75332 | EN 60601-2-45:2011/A2:2024 | Medical electrical equipment - Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices | Standarts spēkā |
| 44345 | LVS EN 60601-3-1:2000 | Medical electrical equipment - Part 3-1: Essential performance requirement for transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment | Standarts spēkā |
| 65864 | EN 62366-1:2015/A1:2020 | Medical devices - Part 1: Application of usability engineering to medical devices | Standarts spēkā |
| 58856 | LVS EN 61675-2:2016 | Radionuclide imaging devices - Characteristics and test conditions - Part 2: Gamma cameras for planar, wholebody, and SPECT imaging | Standarts spēkā |
| 52259 | EN IEC 80601-2-71:2018 | Medical electrical equipment - Part 2-71: Particular requirements for the basic safety and essential performance of functional near-infrared spectroscopy (NIRS) equipment | Standarts spēkā |
| 44631 | EN 60601-2-62:2015 | Medical electrical equipment - Part 2-62: Particular requirements for the basic safety and essential performance of high intensity therapeutic ultrasound (HITU) equipment | Standarts spēkā |
| 55898 | LVS EN 60601-2-23:2016 | Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment | Standarts spēkā |
| 55543 | LVS EN 61262-2:2002 | Medical electrical equipment - Characteristics of electro- optical X-ray image intensifiers - Part 2: Determination of the conversion factor | Standarts spēkā |
| 74843 | EN IEC 80601-2-58:2024 | Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery | Standarts spēkā |
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