Projekta Nr.ISO/IEC Guide 63:2019
Nosaukums<p>This document provides requirements and recommendations to writers of medical device standards on the inclusion of aspects related to safety in International Standards, based on well-established risk management concepts and methodology.</p> <p>This document is applicable to any aspect related to the safety of people, property, the environment, or a combination of these.</p> <p>In this document, the term "product" includes a medical device or a system consisting of one or more medical devices, possibly combined with non-medical devices.</p>
Reģistrācijas numurs (WIID)67944
Darbības sfēra<p>This document provides requirements and recommendations to writers of medical device standards on the inclusion of aspects related to safety in International Standards, based on well-established risk management concepts and methodology.</p> <p>This document is applicable to any aspect related to the safety of people, property, the environment, or a combination of these.</p> <p>In this document, the term "product" includes a medical device or a system consisting of one or more medical devices, possibly combined with non-medical devices.</p>
StatussAtcelts
ICS grupa01.120
11.040.01