DSF/PREN ISO 18113-4
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)
inactive
| Organization: | DS |
| Status: | inactive |
| Page Count: | 19 |
| ICS Code (In vitro diagnostic test systems): | 11.100.10 |
Document History
December 9, 2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing
ISO 18113-4:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for self-testing. ISO 18113-4:2009 also applies to information supplied by...
January 15, 2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing
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...
In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 4: In vitro diagnostic reagents for self-testing (ISO/FDIS 18113-4:2022)
This document specifies requirements for information supplied by the manufacturer of IVD reagents, calibrators, and controls intended for self-testing. This document can also be applied to...
DSF/PREN ISO 18113-4
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)
A description is not available for this item.
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/FDIS 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...
Clinical laboratory testing and in vitro diagnostic medical systems - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/DIS 18113-4:2006)
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self-testing.
Furthermore, this part of ISO 18113 applies to information supplied by...