Superseded
, Reaffirmed
Standard
Historical
ISO 18113-3:2009 (R2015)
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)
Part 3: In vitro diagnostic instruments for professional use
Part 3: In vitro diagnostic instruments for professional use
Summary
ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use. ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use. ISO 18113-3:2009 can also be applied to accessories, where appropriate.
Notes
95.99 : Annulation de la Norme internationale
Technical characteristics
| Publisher | International Organization for Standardization (ISO) |
| Publication Date | 12/09/2009 |
| Confirmation Date | 08/05/2015 |
| Edition | 1 |
| Page Count | 9 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
No products.
Previous versions
09/12/2009
Superseded
, Reaffirmed
Historical