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ISO 18113-1:2009

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

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

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Full Description

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.

 

Product Details

Published:
12/15/2009
File Size:
1 file , 500 KB
Same As:
BS EN ISO 18113-1:2009, DIN EN ISO 18113-1, BS EN ISO 18113-1:2011, DIN EN ISO 18113-1, BS EN ISO 18113-1:2011
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This product is unavailable in Ukraine, Russia, Belarus
 

Document History

  1. ISO 18113-1:2022


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

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  2. ISO 18113-1:2009

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

    • Historical Version