Superseded
Standard
Historical
DIN EN ISO 18113-1:2010-05
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2009.
Preview
Summary
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 1: Begriffe und allgemeine Anforderungen (ISO 18113-1:2009); Deutsche Fassung EN ISO 18113-1:2009 / Achtung: Übergangsfrist, festgelegt durch DIN EN ISO 18113-1 (2013-01), bis 2014-10-31 beachten.
Notes
A transition period, as set out in DIN EN ISO 18113-1 (2013-01), exists until 2014-10-31.
Technical characteristics
| Publisher | Deutsche Institut für Normung e.V. (DIN) |
| Publication Date | 05/01/2010 |
| Page Count | 8 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
No products.
Previous versions
