BS EN ISO 14971:2009
Superseded
View Superseded by
Medical devices. Application of risk management to medical devices
Hardcopy , PDF
English
02-28-2011
07-31-2012
| Committee |
CH/210/4
|
| DocumentType |
Standard
|
| Pages |
96
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
This International Standard 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 this International Standard are applicable to all stages of the life-cycle of a medical device.
This International Standard does not apply to clinical decision making.
This International Standard does not specify acceptable risk levels.
This International Standard does not require that the manufacturer have a quality management system in place. However, risk management can be an integral part of a quality management system.
| Standards | Relationship |
| ISO 14971:2007 | Identical |
| EN ISO 14971:2009 | Identical |
| DIN EN ISO 14971:2009-10 | Equivalent |
| I.S. EN ISO 14971:2009 | Equivalent |
| EN ISO 14971:2009 | Equivalent |
| UNE-EN ISO 14971:2009 | Equivalent |
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