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New Resolution regarding medical devices’ risk classification and regularization comes into force

Date: 03/01/2023

 

Starting today – March 1st 2023 – the new Resolution RDC nº 751/2022  comes into force. The Resolution provides for risk classification, Notification and Registro processes, and the requirements for medical devices’ labeling and instructions for use.

In order to meet the new requirements and procedures, ANVISA has already made available new forms for Notification and Registro, as well as updated the list of necessary documents for the regularization of medical devices in Brazil.

Click here to read the full article containing more information on major updates and highlights prepared by our team.

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DOMO Salute Team

 

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