Standard
withdrawn: DIN EN 61326-2-6 VDE 0843-20-2-6:2013-09Electrical equipment for measurement, control and laboratory use – EMC requirements Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment |
Standard
withdrawn: DIN EN ISO 80601-2-13 VDE 0750-2-13:2013-03Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation |
Anwendungsregel:
VDE-AR-E 2750-200 Anwendungsregel:2013-03Approach to the classification of medical devices and the selection of conformity assessment procedure
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Standard
withdrawn: DIN EN 60601-2-4 VDE 0750-2-4:2012-05Medical electrical equipment Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators |
Standard
withdrawn: DIN EN 60601-2-37 VDE 0750-2-37:2012-05Medical electrical equipment Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment An english translation of this document is available. |
Standard
withdrawn: DIN EN 50527-2-1 VDE 0848-527-2-1:2012-05Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical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; An english translation of this document is available. |
Standard
withdrawn: DIN EN 60601-2-31 VDE 0750-2-31:2012-04Medical electrical equipment Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source |
Standard
withdrawn: DIN EN 60601-2-54 VDE 0750-2-54 Berichtigung 3:2012-04Corrigendum to DIN EN 60601-2-54 (VDE 0750-2-54):2010-05
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Standard
withdrawn: DIN EN 60601-2-45 VDE 0750-2-45:2012-03Medical electrical equipment Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices |
Standard
withdrawn: DIN EN ISO 80601-2-55 VDE 0750-2-55:2012-03Medical electrical equipment Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors |
Standard
withdrawn: DIN EN ISO 80601-2-12 VDE 0750-2-12:2012-02Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators |
Standard
withdrawn: DIN EN ISO 80601-2-61 VDE 0750-2-61:2012-01Medical electrical equipment Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment |
Standard
withdrawn: DIN EN 60601-2-54 VDE 0750-2-54 Berichtigung 2:2011-12Corrigendum to DIN EN 60601-2-54 (VDE 0750-2-54):2010-05; (IEC-Cor.:2011 to IEC 60601-2-54:2009)
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Standard
withdrawn: DIN EN 60601-1-11 VDE 0750-1-11 Berichtigung 1:2011-11Corrigendum to DIN EN 60601-1-11 (VDE 0750-1-11):2011-03; (IEC-Cor.:2011 to IEC 60601-1-11:2010)
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Standard:
DIN EN 60601-2-57 VDE 0750-2-57:2011-11Medical electrical equipment Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use |
Standard
withdrawn: DIN EN 80001-1 VDE 0756-1:2011-11Application of risk management for IT-networks incorporating medical devices Part 1: Roles, responsibilities and activities |
Anwendungsregel
withdrawn: VDE-AR-E 2757-2 Anwendungsregel:2011-08Service Staying at Home Requirements for suppliers of combined services An english translation of this document is available. |
Standard
withdrawn: DIN EN 60601-2-33 VDE 0750-2-33:2011-07Medical electrical equipment Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis |
Standard
withdrawn: DIN EN 80601-2-30 VDE 0750-2-30:2011-05Medical electrical equipment Part 2-30: Particular requirements for the basic safety and essential performance of automated type non-invasive sphygmomanometers |
Standard
withdrawn: DIN EN 60601-1-11 VDE 0750-1-11:2011-03Medical electrical equipment Part 1-11: General requirements for basic safety and essential performance – Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment |