Standard
withdrawn: DIN EN 60601-1 VDE 0750-1 Berichtigung 1:2008-08Corrigenda to DIN EN 60601-1 (VDE 0750-1):2007-07
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Standard
withdrawn: DIN EN 60601-2-33 VDE 0750-2-33:2008-07Medical electrical equipment Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis |
Standard
withdrawn: DIN EN 60601-1-6 VDE 0750-1-6:2008-02Medical electrical equipment Part 1-6: General requirements for basic safety and essential performance – Collateral Standard: Usability |
Standard
withdrawn: DIN EN 60601-1-8 VDE 0750-1-8:2008-02Medical electrical equipment Part 1-8: General requirements for basic safety and essential performance – Collateral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 |
Standard
withdrawn: DIN EN 60601-1-2 VDE 0750-1-2:2007-12Medical electrical equipment Part 1-2: General requirements for basic safety and essential performance – Collateral standard: Electromagnetic compatibility – Requirements and tests |
Standard:
DIN EN 60601-2-22 VDE 0750-2-22 Beiblatt 1:2007-10Safety of laser products Guidelines for the safe use of laser beams on humans |
Standard
withdrawn: DIN EN 60601-2-2 VDE 0750-2-2:2007-09Medical electrical equipment Part 2-2: Particular requirements for the safety of high frequency surgical equipment |
Standard
withdrawn: DIN EN 60601-1 VDE 0750-1:2007-07Medical electrical equipment Part 1: General requirements for basic safety and essential performance |
Standard
withdrawn: DIN EN 60601-2-13 VDE 0750-2-13:2007-05Medical electrical equipment Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems |
Standard
withdrawn: DIN EN 60601-2-27 VDE 0750-2-27 Berichtigung 1:2007-05Corrigenda to DIN EN 60601-2-27 (VDE 0750-2-27):2006-08
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Standard
withdrawn: DIN EN 60601-2-12 VDE 0750-2-12:2007-03Medical electrical equipment Part 2-12: Particular requirements for the safety of lung ventilators - Critical care ventilators |
Standard
withdrawn: DIN EN 60601-1-8 VDE 0750-1-8 Berichtigung 1:2006-12Corrigenda to DIN EN 60601-1-8 (VDE 0750-1-8):2006-11
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Standard
withdrawn: DIN EN 60601-1-8 VDE 0750-1-8:2006-11Medical electrical equipment Part 1-8: General requirements for safety - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems |
Standard
withdrawn: DIN EN 60601-1-2 VDE 0750-1-2:2006-10Medical electrical equipment Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests |
Standard
withdrawn: DIN EN 60601-2-27 VDE 0750-2-27:2006-08Medical electrical equipment Part 2-27: Particular requirements for the safety, including essential performance, of electrocardiographic monitoring equipment |
Standard
withdrawn: DIN EN 60601-2-33 VDE 0750-2-33:2006-08Medical electrical equipment Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis |
Standard
withdrawn: DIN EN 60601-2-4 VDE 0750-2-4 Berichtigung 2:2005-11Corrigenda to DIN EN 60601-2-4 (VDE 0750-2-4):2003-07
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Standard
withdrawn: DIN EN 60601-2-11 VDE 0750-2-11 Berichtigung 1:2005-07Corrigenda to DIN EN 60601-2-11 (VDE 0750-2-11):2005-04
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Standard
withdrawn: DIN EN 60601-1-6 VDE 0750-1-6:2005-06Medical electrical equipment Part 1-6: General requirements for safety - Collateral standard: Usability |
Standard
withdrawn: DIN EN 60601-2-11 VDE 0750-2-11:2005-04Medical electrical equipment Part 2-11: Particular requirements for the safety of gamma beam therapy equipment |