Revision history of "File:HC medical device FRN Form FINAL 2021-05-28.pdf"

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  • curprev 15:07, 1 June 2021‎ Hc.mdd.postmarket-postcommercialisation.dim.sc talk contribs‎ 329 bytes +329‎ This form is intended to be used by manufacturers and importers to report information concerning actions taken in certain foreign jurisdictions to eliminate or mitigate a serious risk of injury to human health related to the use of a medical device, as per sections 61.2 and 61.3 of the Medical Devices Regulations.
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