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MDR system |
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MDR system Medical Device Reporting system FDA A program requiring manufacturers and importers of medical devices to inform the FDA should they receive information suggesting that one of their devices may have caused/contributed to
death/serious injury. See Medical device. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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