Brazil - Draft Resolution 1420, September 23, 2026 on Good Practices for Healthcare Medical Device Processing
Business description
The Brazilian Health Regulatory Agency (ANVISA) has issued Draft Resolution No. 1420, dated September 23, 2026, establishing Good Practice requirements for the processing of medical devices used in healthcare services.
The proposed regulation aims to minimize inconsistencies in device classification and processing practices, strengthen patient safety, reinforce validation and traceability requirements, clarify the responsibilities of involved parties, and support harmonized supervision under the National Health Surveillance System.
Countries:
Brazil
Product categories:
05 Medical Devices
Technical aspects:
Safety
Business fields:
P.05 Medical
Regions:
South-America
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