Abstract
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.
General information
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Status: WithdrawnPublication date: 2009-12Stage: Withdrawal of International Standard [95.99]
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Edition: 1Number of pages: 49
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Technical Committee :ISO/TC 212ICS :11.100.10
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Life cycle
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Now
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Revised by
PublishedISO 18113-1:2022