Abstract
Ïã¸ÛÁùºÏ²Ê¿ª½± 14971:2007 specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.
The requirements of Ïã¸ÛÁùºÏ²Ê¿ª½± 14971:2007 are applicable to all stages of the life-cycle of a medical device.
General information
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Status: WithdrawnPublication date: 2007-03
Corrected version (en): 2007-09
Corrected version (fr): 2007-09Stage: Withdrawal of International Standard [95.99] -
Edition: 2Number of pages: 82
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Technical Committee :Ïã¸ÛÁùºÏ²Ê¿ª½±/TC 210ICS :11.040.01
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Life cycle
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Previously
WithdrawnÏã¸ÛÁùºÏ²Ê¿ª½± 14971:2000
WithdrawnÏã¸ÛÁùºÏ²Ê¿ª½± 14971:2000/Amd 1:2003
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Now
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Revised by
PublishedÏã¸ÛÁùºÏ²Ê¿ª½± 14971:2019
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