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Analysis finds cardiac devices recalled for safety reasons infrequently subjected to premarket or postmarket testing

A cross-sectional study of cardiovascular devices found that most recalled devices did not undergo clinical testing before authorization and were not required to undergo postmarket surveillance studies. The study highlights the need for more rigorous testing and monitoring of these devices to ensure patient safety.

SourceAmerican College of Physicians·JournalAnnals of Internal Medicine·TypeNews article·DateSep 16, 2024

Improving the power transfer efficiency and reducing the magnetic field leakage of pacemaker MCR-WPT system simultaneously via MNG-MNZ metamaterial

Researchers designed a hybrid metamaterial slab for cardiac pacemakers, achieving an efficiency of 62.39% at 20mm transmission distance. The structure also showed superior magnetic leakage shielding performance in finite element simulations.

SourceCES Transactions on Electrical Machines and Systems·JournalCES Transactions on Electrical Machines and Systems·TypeExperimental study·DateJun 24, 2024