ISO/TS 20993:2006
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ISO/TS 20993:2006
36403

Abstract 

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.


General information 

  •  :  Withdrawn
     : 2006-08
  •  : 1
     : 4
  •  : ISO/TC 194 Biological and clinical evaluation of medical devices
  •  :
    11.100.20 Biological evaluation of medical devices

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