DIN EN ISO 18113-4
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
inactive
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| Organization: | DIN |
| Publication Date: | 1 May 2010 |
| Status: | inactive |
| Page Count: | 21 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
Document History
September 1, 2021
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/DIS 18113-4:2021); German and English version prEN ISO 18113-4:2021
A description is not available for this item.
January 1, 2013
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self-testing.
This part of ISO 18113 also applies to information supplied by the...
DIN EN ISO 18113-4
May 1, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
A description is not available for this item.
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