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Brief
"On 27/03/2025, the National Health Surveillance Agency (Anvisa) issued an update regarding Anvisa opens public consultation on database for unique identification of medical devices. The agency aims to facilitate patient safety through international Unique Device Identification (UDI) standards, established by RDC nº 591/2021. A proposed instruction normative outlines conditions for sending UDI data to the Anvisa, with companies having 3.5-6 years to comply depending on device classification."
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