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DIN-EN-ISO-18113-2 - 2010 EDITION - SUPERSEDED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 18113-2:2010-05

Revision Level

2010 EDITION

Status

Superseded

Publication Date

May 1, 2010