This content is provided by LNE
Over the last ten years, the number of MRI scanners in the world has doubled. This means that during his/her lifetime, a human being can undergo an average of four MRI scans. Besides, there is an increasing variety of medical devices likely to be introduced or used in a MRI environment (surgical implant, active implant, vital-sign monitoring devices, stretchers or wheelchairs).
This is the reason why, when a new medical device is marketed, European notified bodies or foreign certification bodies ask to consider an assessment of the risks related to the introduction of the medical device in a MRI environment.
How to proceed? Our webinar, led by Healtis, LNE’s partner company for these issues, will answer that question:
- Risks related to the introduction of a MD in a MRI environment,
- Regulatory aspects of MRI compatibility,
- Risk assessment, MRI compatibility tests.