ISO/TS 20993:2006 describes a process by which a manufacturer can identify the biological hazards associated with medical devices, estimate and evaluate the risks, control these risks and monitor the effectiveness of the control.
Status : WithdrawnPublication date : 2006-08
Edition : 1Number of pages : 4
Technical Committee:Biological and clinical evaluation of medical devices
A standard is reviewed every 5 years
Revisions / Corrigenda