Standard
withdrawn: DIN EN 60601-2-41 VDE 0750-2-41:2001-11Medical electrical equipment Particular requirements for the safety of surgical luminaires and luminaires for diagnosis |
Standard
withdrawn: DIN EN 60601-2-2 VDE 0750-2-2:2001-08Medical electrical equipment Particular requirements for the safety of high frequency surgical equipment |
Standard
withdrawn: DIN EN 60601-2-38 VDE 0750-2-38:2001-07Medical electrical equipment Particular requirements for the safety of electrically operated hospital beds |
Standard
withdrawn: DIN EN 60601-1-4 VDE 0750-1-4:2001-04Medical electrical equipment General requirements for safety - Collateral standard: Programmable electrical medical systems |
Standard
withdrawn: DIN EN 60601-2-25 VDE 0750-2-25:2001-04Medical electrical equipment Particular requirements for the safety of electrocardiographs |
Standard
withdrawn: DIN EN 60601-2-30 VDE 0750-2-30:2000-12Medical electrical equipment Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment |
Standard
withdrawn: DIN EN 60601-2-23 VDE 0750-2-23:2000-11Medical electrical equipment Particular requirements for the safety, including essential performance of transcutaneous partial pressure monitoring equipment |
Standard
withdrawn: DIN EN 60601-2-7 VDE 0750-2-7:2000-03Medical electrical equipment Particular requirements for the safety of high voltage generators of diagnostic X-ray generators |
Standard
withdrawn: DIN EN 60601-2-45 VDE 0750-2-45:2000-03Medical electrical equipment Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices |
Standard
withdrawn: DIN EN 60601-2-39 VDE 0750-2-39:2000-02Medical electrical equipment Particular requirements for the safety for peritoneal dialysis equipment |
Standard
withdrawn: DIN EN 60601-2-3 VDE 0750-2-3:1999-10Medical electrical equipment Particular requirements for the safety of short-wave therapy equipment |
Standard
withdrawn: DIN EN 60601-2-9 VDE 0750-2-9:1999-10Medical electrical equipment Particular requirements for the safety of patient contact dosemeters used in radiotherapy with electrically connected radiation detectors |
Standard
withdrawn: DIN EN 60601-2-31/A1 VDE 0750-2-31/A1:1999-05Medical electrical equipment Particular requirements for the safety of external cardiac pacemakers with internal power source |
Standard
withdrawn: DIN EN 60601-2-16 VDE 0750-2-16:1999-02Medical electrical equipment Particular requirements for safety of haemodialysis, haemodiafiltration and haemofiltration equipment |
Standard
withdrawn: DIN EN 60601-2-24 VDE 0750-2-24:1999-02Medical electrical equipment Particular requirements for the safety of infusion pumps and controllers |
Standard
withdrawn: DIN EN 60601-2-46 VDE 0750-2-46:1999-02Medical electrical equipment Particular requirements for the safety of operating tables |
Standard
withdrawn: DIN EN 60601-2-40 VDE 0750-2-40:1998-12Medical electrical equipment Particular requirements for the safety of electromyographs and evoked response equipment |
Standard
withdrawn: DIN EN 60118-13 VDE 0750-11:1998-12Hearing aids Electromagnetic compatibility (EMC) |
Standard
withdrawn: DIN EN 60601-2-23 VDE 0750-2-23:1998-11Medical electrical equipment Particular requirements for the safety of transcutaneous partial pressure monitoring equipment |
Standard
withdrawn: DIN EN 45502-1 VDE 0750-10:1998-07Active implantable medical devices General requirements for the safety, marking and information to be provided by the manufacturer; |