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# Medical Device Covid FAQs
- URL: https://www.fdaweb.com/medical-device-covid-faqs/
- Published: 2020-08-13T12:00:00.000Z
- Updated: 2026-09-14T16:24:56.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147426

FDA has published two frequently asked questions documents relating to medical device issues during the Covid-19 pandemic.

*Registration and Listing of Medical Devices During the Covid-19 Pandemic* provides [information](https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/registration-and-listing-medical-devices-during-covid-19-pandemic?ref=fdaweb.com) for medical device establishments, including owners and operators of places of business that are involved in the production and distribution of medical devices covered by emergency use authorizations or are the subject of one of the agency’s Covid-19 guidances.

*Importing Medical Devices During the Covid-19 Pandemic* describes [procedures](https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/importing-medical-devices-during-covid-19-pandemic?ref=fdaweb.com) for importing medical devices that have been issued emergency use authorizations and for devices for which an enforcement discretion policy has been published in guidance.