AENOR - UNE-EN ISO 18113-3
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
inactive
| Organization: | AENOR |
| Publication Date: | 7 July 2010 |
| Status: | inactive |
| Page Count: | 18 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
Document History
February 22, 2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
A description is not available for this item.
UNE-EN ISO 18113-3
July 7, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
A description is not available for this item.