NS EN ISO 14971 : 2012
Withdrawn
Withdrawn
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007, CORRECTED VERSION 2007-10-01)
Published date
01-12-2013
Withdrawn date
03-01-2020
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Defines 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.
| DevelopmentNote |
Supersedes NS EN 1441. (11/2006)
|
| DocumentType |
Standard
|
| PublisherName |
Norwegian Standards (Norges Standardiseringsforbund)
|
| Status |
Withdrawn
|
| Standards | Relationship |
| ISO 14971:2007 | Identical |
| NBN EN ISO 14971 : 2012 | Identical |
| NEN EN ISO 14971 : 2007 + COR 2012 | Identical |
| I.S. EN ISO 14971:2012 | Identical |
| BS EN ISO 14971:2012 | Identical |
| EN ISO 14971:2012 | Identical |
| DIN EN ISO 14971:2013-04 | Identical |
| UNE-EN ISO 14971:2012 | Identical |
| NF EN ISO 14971 : 2009-11 | Identical |
Summarise
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