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ISO 18113-3:2009
In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 3: In vitro diagnostic instruments for professional use
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Abstract
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.
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Edition: 1 (Monolingual) ICS: 11.100.10 Status: Published Stage: 60.60 (2009-12-09) TC/SC: ISO/TC 212 Number of Pages: 9 -
No revision information available
