MDR Data Files | FDA
Older medical device reports received through the Alternative Summary Reporting program and Device Experience Network (DEN) reporting system are available.| U.S. Food and Drug Administration
Older medical device reports received through the Alternative Summary Reporting program and Device Experience Network (DEN) reporting system are available.| U.S. Food and Drug Administration
Post Market Surveillance (PMS) monitors medical device safety and effectiveness post-market. what's new in 2024?| Sternum IoT
The Pittsburgh Post-Gazette and ProPublica analyzed more than 2 million complaints about medical device malfunctions, patient injuries and deaths submitted to the U.S. Food and Drug Administration’s MAUDE tracking system.| newsinteractive.post-gazette.com
Requirements for reporting medical device problems, including malfunctions and adverse events (serious injuries or deaths) associated with medical devices.| U.S. Food and Drug Administration
These early adopters found out what happened when a cutting-edge marvel became an obsolete gadget... inside their bodies.| IEEE Spectrum
