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 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:
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 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 50527-1 VDE 0848-527-1:2017-12Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 1: General; |
Standard:
DIN EN 50527-2-1 VDE 0848-527-2-1:2017-12Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices Part 2-1: Specific assessment for workers with cardiac pacemakers; |
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 |
Standard:
DIN EN 60601-2-3 VDE 0750-2-3:2017-10Medical electrical equipment Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment |
Standard:
DIN EN 60601-2-6 VDE 0750-2-6:2017-10Medical electrical equipment Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment |
Standard:
DIN EN 60601-2-10 VDE 0750-2-10:2017-09Medical electrical equipment Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators |
Standard:
DIN EN 62471 VDE 0837-471 Beiblatt 3:2017-06Photobiological safety of lamps and lamp systems Supplement 3: Guidelines for the safe use of intense pulsed light source equipment on humans |
Standard:
DIN EN 60601-2-44 VDE 0750-2-44:2017-03Medical electrical equipment Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography |