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- May 08, 2026FDA Updates Import Rules for AI Diagnostic Devices (Oct 2026)FDA's new AI diagnostic import rules require Algorithm Traceability Reports (ART) from Oct 2026 — essential for exporters, regulators & supply chains. Act now.Posted by:Medical Device Expert
- May 08, 2026Air quality monitors that miss VOC spikes can mislead roomsAir quality monitors can miss short VOC spikes and make enclosed rooms seem safer than they are. Learn the key checks for accurate data, safer decisions, and smarter monitor selection.Posted by:Medical Device Expert
- May 07, 2026ANVISA Updates Rehab Devices Registration: Remote Robots Require Local Clinical DataANVISA now requires local clinical data for rehab devices—exoskeletons, neurofeedback & VR systems—registering in Brazil. Act before the 90-day deadline!Posted by:Medical Device Expert
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