Superseded
Standard
Historical
DIN EN ISO 18113-3:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011.
Summary
This part of DIN EN ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for professional use. Furthermore, this part of DIN EN ISO 18113 also applies to apparatus and equipment intended to be used with IVD instruments for professional use. This part of DIN EN ISO 18113 can also be applied to accessories, where appropriate.
Notes
DIN EN ISO 18113-3 (2010-05) remains valid alongside this standard until 2014-10-31.
Technical characteristics
| Publisher | Deutsche Institut für Normung e.V. (DIN) |
| Publication Date | 01/01/2013 |
| Page Count | 18 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
No products.
Previous versions
01/02/2007
Superseded
Historical