With the publication of RDC No. 591/2021, ANVISA is regulating the Unique Identification of Medical Devices (UDI) system that must be complied with by manufacturers and notification or registration holders for the identification of medical products and products for in vitro diagnostics.
Marianne Albers and Thaís Fernandes have published an Alert explaining the UDI, its composition, and implementation in our country.
Read the full content, in Portuguese, at: https://bit.ly/34PSP8L
