DIN-EN-ISO-18113-1 › In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

DIN-EN-ISO-18113-1 - 2013 EDITION - CURRENT
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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)


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Document Number

DIN EN ISO 18113-1:2013-01

Revision Level

2013 EDITION

Status

Current

Publication Date

Jan. 1, 2013