CEN - EN ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
inactive
| Organization: | CEN |
| Publication Date: | 1 December 2009 |
| Status: | inactive |
| Page Count: | 60 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
Document History
October 1, 2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.
This part of ISO...
EN ISO 18113-1
December 1, 2009
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.