In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use

ISO 18113-3:2009

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use

This international standard specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.

This document is available in electronic format only. 

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Publication Details

Date of Publication: December 1, 2009

Order Code PDF: ISO181133E

Order Code Print: print not available

Edition: First

Pages: 9

ISO 18113-3:2009 Additional Details

The document also applies to apparatus and equipment intended to be used with IVD instruments for professional use.

Technical Committee: ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems