Superseded , Reaffirmed Standard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

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.