AENOR - UNE-EN ISO 18113-2
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
active, Most Current
| Organization: | AENOR |
| Publication Date: | 22 February 2012 |
| Status: | active |
| Page Count: | 20 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
| ICS Code (Other standards related to laboratory medicine): | 11.100.99 |
Document History
UNE-EN ISO 18113-2
February 22, 2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
A description is not available for this item.
June 16, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
A description is not available for this item.