ISO 18113-1:2009 (R2015)
Superseded , Reaffirmed Standard
Historical

ISO 18113-1:2009 (R2015)

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)
Part 1: Terms, definitions and general requirements
Most recent standard

Summary

ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.

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 49
EAN ---
ISBN ---
Weight (in grams) ---
No products.

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