ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.
ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
ISO 18113-3:2009 can also be applied to accessories, where appropriate.
Status: WithdrawnPublication date: 2009-12
Edition: 1Number of pages: 9
Technical Committee: ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems