Medical Device Reporting (MDR)

Medical Device Reporting (MDR) is a system used by manufacturers, healthcare providers, and others to report when a medical device may have caused or contributed to a health problem or injury, or if it is defective and could pose a risk. This process helps regulatory agencies monitor the safety and performance of medical devices, ensuring issues are identified and addressed promptly to protect patient health and safety. MDR is a critical part of maintaining trust in medical devices and fostering continuous improvement in their safety and effectiveness.