BSI - BS EN ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) -Part 1: Terms, definitions and general requirements
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| Organization: | BSI |
| Publication Date: | 31 October 2011 |
| Status: | active |
| Page Count: | 62 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
Document History
August 11, 2021
Draft BS EN ISO 18113-1 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling). Part 1: Terms, definitions, and general requirements
A description is not available for this item.
BS EN ISO 18113-1
October 31, 2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) -Part 1: Terms, definitions and general requirements
A description is not available for this item.
October 31, 2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) Part 1: Terms, definitions and general requirements
A description is not available for this item.
February 28, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) Part 1: Terms, definitions and general requirements
A description is not available for this item.
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