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 |
|
Standard:
DIN EN IEC 60601-2-46 VDE 0750-2-46:2020-04Medical electrical equipment Part 2-46: Particular requirements for the basic safety and essential performance of operating tables |
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:
DIN EN ISO 20342-1 VDE 0750-2-52-1:2020-03Assistive products for tissue integrity when lying down Part 1: General Requirements |
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 |
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 |
Draft:
E DIN IEC 63203-401-1 VDE 0750-33-1:2019-03Wearable electronic devices and technologies Part 401-1: Devices and Systems – Functional elements – Evaluation method of the stretchable resistive strain sensor |
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 |
Standard:
DIN EN 50637 VDE 0750-212:2018-07Medical electrical equipment Particular requirements for the basic safety and essential performance of medical beds for children; |
|
Standard:
DIN EN 82304-1 VDE 0750-102-1:2018-04Health Software Part 1: General requirements for product safety |
Standard:
DIN EN 60601-2-64 VDE 0750-2-64:2018-01Medical electrical equipment Part 2-64: Particular requirements for the basic safety and essential performance of light ion beam medical electrical equipment |
Standard:
DIN EN 60601-2-33 VDE 0750-2-33:2017-11Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |