In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 2: In vitro diagnostic reagents for professional use
This standard was last reviewed and confirmed* in 2015.
ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.
ISO 18113-2:2009 can also be applied to accessories.
ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.
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: 10
This standard has not been revised
No corrigenda or amendments available