JIS T 14971:2012Medical devices - Application of risk management to medical devices
Abstract
This Japanese Industrial Standard specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic 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 Standard are applicable to all stages of the life-cycle of a medical device.
Details
| Status |
Current |
| Pages |
88 |
| Language |
English |
| Supersedes |
JIS T 14971:2003 |
| Superseded By |
|
| DocumentFormat |
PDF(Copy/Paste/Networkable) |
| Published |
01-03-2012 |
| History |
2012(R2016) [25/10/2016]
2012 [01/03/2012]
2003(R2009) [25/04/2009]
2003 [25/08/2003] |
Note
We will send the latest version to you, please contact us if you want the exact document as the title. Some old Standards are in scancopy and no reaffirmed stamp
This product was added to our catalog on Saturday 10 March, 2018.
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