Abstract
ISO/TS 19218:2005 specifies requirements for a coding structure for describing adverse events related to medical devices. This code is intended for use by medical device users, manufacturers and regulatory authorities.
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Status: WithdrawnPublication date: 2005-11
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Edition: 1Number of pages: 11
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Technical Committee: ISO/TC 210 Quality management and corresponding general aspects for products with a health purpose including medical devices
Life cycle
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Now
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Revised by
WithdrawnISO/TS 19218-1:2011
WithdrawnISO/TS 19218-2:2012
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