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Registration of a medical device in Brazil free guide
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Registration medical device in Brazil - Free guide

LNE/G-MED has published a guide to help manufacturers understand all the criteria they should respect in order to meet the strict requirements when marketing their products on the Brazilian market.

The guide first presents a reminder of the medical device classification system in force in Brazil, and then describes the 5 steps of the registration procedure to get marketing authorization.

Simply complete the information below. Please be sure to provide a valid email address, so we can send your FREE guide.

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In accordance with French law covering data processing and individual liberties, you are entitled to consult data about yourself and request its correction or deletion. To do this, please send an email to info.gmed@lne.fr

 


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