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.
The document also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
This document is available in electronic format only.
Date of Publication: December 1, 2009
Order Code PDF: ISO181133E
Order Code Print: print not available
ISO 18113-3:2009 Additional Details
Membership discounts cannot be applied to ISO documents because they are not published by CLSI. CLSI is able to offer ISO Technical Committee 212 approved and draft standards through an agreement with the American National Standards Institute.
Technical Committee: ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems