The Manufacturer and User Facility Device Experience (MAUDE) database is a searchable database of medical device reports (MDRs) of adverse events involving medical devices over the last ten years. Reports older than ten years are provided on the FDA’s MDR Data Files webpage. Read more…
Yearly Archives: 2025
3 posts
Shortages of medical devices can occur for many reasons, including manufacturing and quality problems, geopolitical issues, natural disasters, delays, public health emergencies (PHEs), and discontinuations. The Office of Supply Chain Resilience (OSCR), in the CDRH Office of Strategic Partnerships & Technology Innovation (OST), is responsible for managing the FDA’s activities […]
Medical Device Reprocessing Market by Type (Reprocessed Medical Devices), Device Category (Critical- Devices, Semi-Critical Devices, Non-Critical Devices), Application (Cardiology, Gynecology, Gastroenterology, Anesthesia) – Global Forecast to 2027 Read more…