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withdrawn: DIN EN 60601-1-2 VDE 0750-1-2:2006-10Medical electrical equipment Part 1-2: General requirements for safety - Collateral standard: Electromagnetic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withdrawn: DIN EN 60601-2-27 VDE 0750-2-27:2006-08Medical electrical equipment Part 2-27: Particular requirements for the safety, including essential performance, of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withdrawn: DIN EN 60601-2-33 VDE 0750-2-33:2006-08Medical electrical equipment Part 2-33: Particular requirements for the safety of magnetic resonance equipment for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withdrawn: DIN EN ISO 21647 VDE 0750-2-55 Berichtigung 2:2006-07Corrigenda to DIN EN ISO 21647 (VDE 0750-2-55):2005-06
|
Standard
withdrawn: DIN EN 60118-13 VDE 0750-11:2006-03Electroacoustics - Hearing aids Part 13: Electromagnetic compatibility (EMC) |
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withdrawn: DIN EN 60601-2-4 VDE 0750-2-4 Berichtigung 2:2005-11Corrigenda to DIN EN 60601-2-4 (VDE 0750-2-4):2003-07
|
Standard
withdrawn: DIN EN ISO 21647 VDE 0750-2-55 Berichtigung 1:2005-11Corrigenda to DIN EN ISO 21647 (VDE 0750-2-55):2005-06
|
Standard
withdrawn: DIN EN ISO 9919 VDE 0750-2-54:2005-09Medical electrical equipment Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
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withdrawn: DIN EN 60601-2-11 VDE 0750-2-11 Berichtigung 1:2005-07Corrigenda to DIN EN 60601-2-11 (VDE 0750-2-11):2005-04
|
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withdrawn: DIN EN 60601-1-6 VDE 0750-1-6:2005-06Medical electrical equipment Part 1-6: General requirements for safety - Collateral standard: Usability |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withdrawn: DIN EN ISO 21647 VDE 0750-2-55:2005-06Medical electrical equipment Particular requirements for the basic safety and essential performance of respiratory gas monitors |
|
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withdrawn: DIN EN 60601-2-11 VDE 0750-2-11:2005-04Medical electrical equipment Part 2-11: Particular requirements for the safety of gamma beam therapy equipment |
Standard
withdrawn: DIN EN 60601-2-17 VDE 0750-2-17:2004-12Medical electrical equipment Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment |
Standard
withdrawn: DIN EN 60601-1-8 VDE 0750-1-8:2004-09Medical electrical equipment Part 1-8: General requirements for safety - Collateral standard: General requirements, tests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withdrawn: DIN EN 60601-2-4 VDE 0750-2-4 Berichtigung 1:2004-08Corrigenda to DIN EN 60601-2-4 (VDE 0750 Teil 2-4):2003-07
|
Standard
withdrawn: DIN EN 45502-2-1 VDE 0750-10-1:2004-08Active implantable medical devices Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers); |
Standard
withdrawn: DIN EN 60601-2-44 VDE 0750-2-44:2004-04Medical electrical equipment Part 2-44: Particular requirements for the safety of X-ray equipment for computed tomography |
Standard
withdrawn: DIN EN 60601-2-51 VDE 0750-2-51:2004-02Medical electrical equipment Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs |
Standard
withdrawn: DIN EN 60601-2-26 VDE 0750-2-26:2004-01Medical electrical equipment Part 2-26: Particular requirements for the safety of electroencephalographs |