Projekta Nr.ISO 18113-1:2022
Nosaukums<p>This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.</p> <p>This document does not address language requirements since that is the domain of national laws and regulations.</p> <p>This document does not apply to:</p> <p>a) IVD medical devices for performance evaluation (e.g. for investigational use only);</p> <p>b) shipping documents;</p> <p>c) material safety data sheets / Safety Data Sheets;</p> <p>d) marketing information (consistent with applicable legal requirements).</p> <p>.</p>
Reģistrācijas numurs (WIID)79866
Darbības sfēra<p>This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.</p> <p>This document does not address language requirements since that is the domain of national laws and regulations.</p> <p>This document does not apply to:</p> <p>a) IVD medical devices for performance evaluation (e.g. for investigational use only);</p> <p>b) shipping documents;</p> <p>c) material safety data sheets / Safety Data Sheets;</p> <p>d) marketing information (consistent with applicable legal requirements).</p> <p>.</p>
StatussStandarts spēkā
ICS grupa11.100.10