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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

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.

References

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