Standard
withdrawn: DIN EN ISO 80601-2-13/A2 VDE 0750-2-13/A2:2020-06Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation; Amendment 2 |
Standard:
DIN EN 80601-2-58 VDE 0750-2-58:2020-06Medical electrical equipment Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery |
Standard:
DIN EN IEC 60601-2-16 VDE 0750-2-16:2020-05Medical electrical equipment Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment |
Standard:
DIN EN IEC 60601-2-39 VDE 0750-2-39:2020-05Medical electrical equipment Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment |
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Standard:
DIN EN 60601-2-68 VDE 0750-2-68:2020-04Medical 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 equipment |
Standard:
DIN EN IEC 80601-2-30 VDE 0750-2-30:2020-03Medical electrical equipment Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
Standard
withdrawn: DIN EN 60601-2-43 VDE 0750-2-43 Berichtigung 1:2020-03Medical electrical equipment Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures; |
Standard:
DIN EN 60601-2-54 VDE 0750-2-54:2020-03Medical electrical equipment Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy |
Standard:
DIN EN IEC 60601-2-76 VDE 0750-2-76:2020-02Medical electrical equipment Part 2-76: Particular requirements for the basic safety and essential performance of low energy ionized gas haemostasis equipment |
Standard:
DIN EN 50527-2-2 VDE 0848-527-2-2:2019-11Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 2-2: Specific assessment for workers with cardioverter defibrillators (ICDs); |
Standard:
DIN EN IEC 61340-6-1 VDE 0300-6-1:2019-08Electrostatics Part 6-1: Electrostatic control for healthcare – General requirements for facilities |
Draft:
E DIN EN IEC 80601-2-86 VDE 0750-2-86:2019-06Medical electrical equipment Part 2-86: Particular requirements for the basic safety and essential performance of electrocardiographs, including diagnostic equipment, monitoring equipment, ambulatory equipment, electrodes, cables and leadwires |
Draft:
E DIN EN IEC 60601-2-23 VDE 0750-2-23:2019-05Medical electrical equipment Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment |
Standard:
DIN EN 60601-2-40 VDE 0750-2-40:2019-04Medical electrical equipment Part 2-40: Particular requirements for the basic safety and essential Performance of electromyographs and evoked response equipment |
Standard
withdrawn: DIN EN 60601-2-43 VDE 0750-2-43:2019-04Medical electrical equipment Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures |
Standard:
DIN EN IEC 60601-2-2 VDE 0750-2-2:2018-12Medical electrical equipment Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories |
Standard:
DIN EN IEC 80601-2-71 VDE 0750-2-71:2018-12Medical electrical equipment Part 2-71: Particular requirements for the basic safety and essential performance of functional near-infrared spectroscopy (NIRS) equipment |
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Standard
withdrawn: DIN EN 60601-1-8/A11 VDE 0750-1-8/A11:2018-02Medical electrical equipment Part 1-8: General requirements for basic safety and essential performance – Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems; |