a b c d e f g h i j k l m n o p q r s t u v w x y z

safety

freedom from unacceptable risk

Bron

ISO/IEC Guide 51:1999, definition 3.1

Norm
NEN-EN-ISO 18113-1:2011 en
Titel
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
Paragraaf
3.63
Terug

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