Abstract
ISO/TS 20993:2006 describes a process by which a manufacturer can identify the biological hazards associated with medical devices, estimate and evaluate the risks, control these risks and monitor the effectiveness of the control.
General information
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Status: WithdrawnPublication date: 2006-08Stage: Withdrawal of International Standard [95.99]
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Edition: 1Number of pages: 4
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Technical Committee :ISO/TC 194ICS :11.100.20
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