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# FDA Updates Covid MDR Questions, Answers
- URL: https://www.fdaweb.com/fda-updates-covid-mdr-questions-answers/
- Published: 2020-09-09T12:00:00.000Z
- Updated: 2026-09-14T16:28:10.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147619

FDA has updated its Frequently Asked Questions (FAQs) document that explains how a manufacturer distributing medical devices under an emergency use authorization or following a Covid-19 enforcement policy guidance that has not completed registration and listing can sign up for an electronic Medical Device Reporting account and submit medical device reports electronically. The [FAQs](https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/adverse-event-reporting-medical-devices-under-emergency-use-authorization-eua-or-discussed-covid-19?utm%5Fcampaign=2020-09-09%20CDRH%20-%20%20eMDR%20EUA%20update&utm%5Fmedium=email&utm%5Fsource=Eloqua) also include general information on how to submit adverse events reports for the devices.