CEN - EN ISO 18113-2
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
inactive
| Organization: | CEN |
| Publication Date: | 1 December 2009 |
| Status: | inactive |
| Page Count: | 22 |
| 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 2: In vitro diagnostic reagents for professional use
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for professional use.
This part of ISO 18113 also applies to information supplied by the...
EN ISO 18113-2
December 1, 2009
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
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