The Medical Product Safety Network (MedSun) is an adverse event reporting program launched in 2002 by the U.S. Food and Drug Administration s Center for Devices and Radiological Health...

FDA System Use Notification. Warning **** Warning **** Warning. This warning banner provides privacy and security notices consistent with applicable federal laws, directives, and other …

If you have any questions, please call MedSun at (800) 859-9821 or email [email protected].

2025年1月17日 · On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.

You may have heard the terms Mandatory Medical Device Reporting, MedWatch, or MedSun (the Medical Product Safety Network) during your career in the medical field, but do you know what …

In order to reach more deeply into the participating hospitals to obtain incident information from the actual clinical users of the medical devices, MedSun is now implementing targeted …

The U.S. Food and Drug Administration (FDA) is now in its fifth year of identifying medical device-associated risks through the Medical Product Safety Network (commonly known as MedSun). …

MedSun utilizes a secure, on-line system for reporting problems with the use of medical devices. MedSun plays a critical role in FDA’s postmarket surveillance efforts.

The MedSun Program, which was launched in 2002 by the U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH), involves the reporting of problems …

2025年1月17日 · The MedSun program, launched in 2002 by the FDA’s Center for Devices and Radiological Health (CDRH), uses a secure online reporting system to receive medical device …