In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 3: In vitro diagnostic instruments for professional use
This standard was last reviewed and confirmed* in 2015.
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.
Document published on: 2009-12-15 Edition: 1 (Monolingual) ICS: 11.100.10 Status: Published Stage: 90.93 (2015-08-05) TC/SC: ISO/TC 212 Number of Pages: 9
This standard has not been revised
No corrigenda or amendments available