Superseded
, Reaffirmed
Standard
Historical
ISO 18113-4:2009 (R2015)
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)
Part 4: In vitro diagnostic reagents for self-testing
Part 4: In vitro diagnostic reagents for self-testing
Summary
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 the manufacturer with calibrators and control materials intended for use with IVD medical devices for self-testing. ISO 18113-4:2009 can also be applied to accessories, where appropriate. ISO 18113-4:2009 applies to the labels for outer and immediate containers and to the instructions for use.
Notes
95.99 : Annulation de la Norme internationale
Technical characteristics
| Publisher | International Organization for Standardization (ISO) |
| Publication Date | 12/17/2009 |
| Confirmation Date | 08/05/2015 |
| Edition | 1 |
| Page Count | 10 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
No products.
Previous versions
17/12/2009
Superseded
, Reaffirmed
Historical