DIN-EN-ISO-18113-2 › Historical Revision Information
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)

DIN-EN-ISO-18113-2 - 2012 EDITION - SUPERSEDED
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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)


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Document Number

DIN-EN-ISO-18113-2

Revision Level

2012 EDITION

Status

Superseded

Publication Date

April 1, 2012