I'm working on obtaining UDIs, listing GUDID and updating FURLS Product Registration Proprietary Names. (This project is driven by the FDA's Sept. 2020 deadline for Class I products UDI/GUDID requirements.) My company would like to change the names for several products that are already listed in FURLS and have UDIs (name change only - no product change). Can someone point me to FDA information about product names being consistently listed in FURLS, UDI, GUDID and our Company's Website? I realize this is part of labeling, but I haven't found clear guidance on the requirement. And...what happens if we change product names in the future? What are requirements for all 4 listings?