Superseded
Standard
Historical
NBN EN ISO 14971:2009
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
Summary
ISO 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 ISO 14971:2007 are applicable to all stages of the life-cycle of a medical device.
The requirements of ISO 14971:2007 are applicable to all stages of the life-cycle of a medical device.
Technical characteristics
| Publisher | Bureau de Normalisation Belge (NBN) |
| Publication Date | 10/02/2009 |
| Cancellation Date | 03/21/2010 |
| Page Count | 105 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
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Previous versions
29/01/2020
Active
, Modified
Most Recent
19/06/2007
Superseded
Historical