Brazil - Anvisa Draft Update in the Regulation for Risk Classification, Registration Regime and Labeling Requirements and Instructions for Use of Medical Devices.
Business description
The Brazilian Health Regulatory Agency (Anvisa) issued the Public Consultation No. 730 of October 14, 2019, to update the risk classification, registration regime and labeling requirements and instructions for use of medical devices according to Anvisa Resolution RDC No 185 of October 22, 2001.
Contributions are accepted by filling in the specific form in the Anvisa Public Consultation Contributions link between October 30 and December 30, 2019.
Countries:
Brazil
Product categories:
05 Non-Active Medical Devices
Technical aspects:
Labeling and Packaging
Safety
User Manual
Business fields:
P.05 Medical
Regions:
South-America
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