BSI - 21/30416029 DC
Draft BS EN ISO 18113-1 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling). Part 1: Terms, definitions, and general requirements
pending
| Organization: | BSI |
| Publication Date: | 11 August 2021 |
| Status: | pending |
| Page Count: | 61 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
Document History
21/30416029 DC
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.
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.