MAUDE - Manufacturer and User Facility Device ExperienceExplore further
2021-10-31u2002·u2002MAUDE - Manufacturer and User Facility Device Experience. The MAUDE database houses medical device reports submitted to the FDA by mandatory reporters 1 (manufacturers, importers and device user facilities) and voluntary reporters such as health care professionals, patients and consumers. Each year, the FDA receives several hundred thousand ...
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