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ISO 18113-1:2009 (R2015)

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ISO 18113-1:2009 (R2015)

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements

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Author ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
Editor ISO
Document type Standard
Format Paper
Confirmation date 2015-08-05
Edition 1
ICS 11.100.10 : In vitro diagnostic test systems
Number of pages 49
Weight(kg.) 0.1833
Year 2009
Country Switzerland