1667601

ISO 18113-3:2009

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use

standard by International Organization for Standardization , 12/15/2009

This document has been replaced. View the most recent version.

View all product details

Historical

Track It

Language:
    • Available Formats
    • Options
    • Availability
    • Priced From ( in USD )
    • Printed Edition
    • Ships in 1-2 business days
    • $73.00
    • Add to Cart
    • Printed Edition + PDF
    • Immediate download
    • $120.00
    • Add to Cart

Customers Who Bought This Also Bought

Identical Versions Available

 

About This Item

 

Full Description

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.

 

Product Details

Published:
12/15/2009
File Size:
1 file , 180 KB
Same As:
BS EN ISO 18113-3:2009, DIN EN ISO 18113-3, BS EN ISO 18113-3:2011, DIN EN ISO 18113-3
Note:
This product is unavailable in Ukraine, Russia, Belarus
 

Document History

  1. ISO 18113-3:2022


    In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use

    • Most Recent

  2. ISO 18113-3:2009

    👀 currently
    viewing


    In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use

    • Historical Version