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In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
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Available format(s): Hardcopy
Language(s): English
Published date: 21-11-2011
Publisher: Standardiserings-Kommissionen I Sverige
This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.
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