Over deze norm
|Commissie||Medische elektrische toestellen|
This technical report describes the technical requirements for use of equipment in HAEMODIALYSIS, HAEMOFILTRATION and HAEMODIAFILTRATION. These principles should be complied with to ensure safe, permissible and proper application. The physician is responsible for the HAEMODIALYSIS treatment prescription. However, the ORGANIZATION administering the treatment is responsible for all resources, structures and processes used in connection with the treatment. These responsibilities will not be described here. If applicable, the scope may be applicable to the use of the equipment in paediatrics, home HAEMODIALYSIS, acute and SORBENT DIALYSIS SYSTEMS. The requirements of IEC 60601-2-16 ensure that equipment used for extracorporeal renal replacement therapy operates with a high level of safety. Despite that high level of safety, however, some residual risk remains, related to medical-biological, physical-chemical and technical HAZARDS. The ORGANIZATION administering the treatment is responsible for managing the residual risk. This technical report is not intended to be used as the basis of regulatory inspection or certification assessment activities.
|Nederlandse titel||Richtlijn voor het veilig bedienen van medische apparatuur gebruikt voor hemodialysebehandelingen|
|Engelse titel||Guideline for safe operation of medical equipment used for haemodialysis treatments|