1667600

ISO 18113-2:2009

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

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

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Full Description

ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.

ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.

ISO 18113-2:2009 can also be applied to accessories.

ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.

 

Product Details

Published:
12/15/2009
File Size:
1 file , 200 KB
Same As:
BS EN ISO 18113-2:2011, DIN EN ISO 18113-2, DIN EN ISO 18113-2, BS EN ISO 18113-2:2011
Note:
This product is unavailable in Ukraine, Russia, Belarus
 

Document History

  1. ISO 18113-2:2022


    In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

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  2. ISO 18113-2:2009

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    In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

    • Historical Version