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withdrawn: DIN EN 60601-2-23 VDE 0750-2-23:2000-11Medical electrical equipment Particular requirements for the safety, including essential performance of transcutaneous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withdrawn: DIN EN 60601-2-7 VDE 0750-2-7:2000-03Medical electrical equipment Particular requirements for the safety of high voltage generators of diagnostic X-ray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withdrawn: DIN EN 60601-2-45 VDE 0750-2-45:2000-03Medical electrical equipment Particular requirements for the safety of mammographic X-ray equipment and mammographic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withdrawn: DIN EN 60601-2-39 VDE 0750-2-39:2000-02Medical electrical equipment Particular requirements for the safety for peritoneal dialysis equipment |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withdrawn: DIN EN 60601-2-3 VDE 0750-2-3:1999-10Medical electrical equipment Particular requirements for the safety of short-wave therapy equipment |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withdrawn: DIN EN 60601-2-9 VDE 0750-2-9:1999-10Medical electrical equipment Particular requirements for the safety of patient contact dosemeters used in radiotherapy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withdrawn: DIN EN 60601-2-31/A1 VDE 0750-2-31/A1:1999-05Medical electrical equipment Particular requirements for the safety of external cardiac pacemakers with internal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withdrawn: DIN EN 60601-2-16 VDE 0750-2-16:1999-02Medical electrical equipment Particular requirements for safety of haemodialysis, haemodiafiltration and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withdrawn: DIN EN 60601-2-24 VDE 0750-2-24:1999-02Medical electrical equipment Particular requirements for the safety of infusion pumps and controllers |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withdrawn: DIN EN 60601-2-46 VDE 0750-2-46:1999-02Medical electrical equipment Particular requirements for the safety of operating tables |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withdrawn: DIN EN 60601-2-40 VDE 0750-2-40:1998-12Medical electrical equipment Particular requirements for the safety of electromyographs and evoked response equipment |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withdrawn: DIN EN 60601-2-23 VDE 0750-2-23:1998-11Medical electrical equipment Particular requirements for the safety of transcutaneous partial pressure monitoring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withdrawn: DIN EN 60601-2-33/A11 VDE 0750-2-33/A11:1998-02Medical electrical equipment Particular requirements for the safety of magnetic resonance equipment for medical diagnosis |
Standard
withdrawn: DIN EN 60601-2-19 VDE 0750-2-19:1998-01Medical electrical equipment Particular requirements for safety of baby incubators |
Standard
withdrawn: DIN EN 60601-2-20 VDE 0750-2-20:1998-01Medical electrical equipment Particular requirements for safety of transport incubators |
Standard
withdrawn: DIN EN 60601-2-21/A1 VDE 0750-2-21/A1:1998-01Medical electrical equipment Particular requirements for the safety of infant radiant warmers |
Standard
withdrawn: DIN EN 60601-2-38 VDE 0750-2-38:1998-01Medical electrical equipment Particular requirements for the safety of electrically operated hospitals beds |
Standard
withdrawn: DIN EN 60601-2-35 VDE 0750-2-35:1997-12Medical electrical equipment Particular requirements for the safety of blankets, pads, mattresses, intended for heating in medical use |
Standard
withdrawn: DIN EN 60601-2-36 VDE 0750-2-36:1997-12Medical electrical equipment Particular requirements for the safety for extracorporeally induced lithotripsy |
Standard
withdrawn: DIN EN 60601-2-22 VDE 0750-2-22 Berichtigung 1:1997-11Berichtigungen zu DIN EN 60601-2-22 (VDE 0750 Teil 2-22):1996-12
|