Food & Drug Administration manufacturer user facility & distributor experience.
This category page includes the MAUDE data from the Federal Food and Drug Administration which represents reports of adverse events involving medical devices. A document is a report of adverse event involving a medical device.
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| Format: | Online |
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| Language: | English |
| Published: |
[United States] :
[publisher not identified]
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| Subjects: | |
| Online Access: | https://www.westlaw.com/Browse/Home/AdministrativeDecisionsGuidance/FederalAdministrativeDecisionsGuidance/DepartmentofHealthHumanServices/FoodDrugAdministration/FoodDrugAdministrationManufacturerUserFacilityDistributorExperience?rs=tran3.0&vr=3.0&originationContext=vendcc |
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