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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.

References

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