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1. www.accessdata.fda.gov › scripts › cdrhManufacturer and User Facility Device Experience (MAUDE) Database

   www.accessdata.fda.gov › scripts › cdrh

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   Jun 30, 2024 · 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...

2. www.accessdata.fda.gov › scripts › cdrhMAUDE - Manufacturer and User Facility Device Experience

   www.accessdata.fda.gov › scripts › cdrh

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   Jun 30, 2024 · 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...

3. www.fda.gov › medical-devices › mandatory-reporting-requirements-manufacturersAbout Manufacturer and User Facility Device Experience (MAUDE)...

   www.fda.gov › medical-devices › mandatory-reporting-requirements-manufacturers

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   Description of the MAUDE Database. The Manufacturer and User Facility Device Experience (MAUDE) database contains medical device reports (MDRs) of adverse events.

4. www.fda.gov › adverse-event-reporting-data-filesAdverse Event Reporting Data Files | FDA

   www.fda.gov › adverse-event-reporting-data-files

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   Jun 21, 2019 · Information about the Adverse Event Reporting Data Files including Manufacturer and User Facility Device Experience (MAUDE) data and Medical Device Reporting (MDR) data.

5. www.fda.gov › mdr-data-filesMDR Data Files | FDA - U.S. Food and Drug Administration

   www.fda.gov › mdr-data-files

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   Feb 18, 2022 · The FDA makes medical device reports available to patients and health care providers on the FDA's public Manufacturer and User Facility Device Experience (MAUDE) database as one source of ...

6. open.fda.gov › data › maudeManufacturer and User Facility Device Experience

   open.fda.gov › data › maude

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   The MAUDE database houses medical device reports (MDRs) submitted to the FDA by mandatory reporters (manufacturers, importers and device user facilities) and voluntary reporters such as...

7. redica.com › keys-to-accurately-analyzing-fdas-maude-databaseKeys to Accurately Analyzing FDA’s MAUDE Database

   redica.com › keys-to-accurately-analyzing-fdas-maude-database

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   Apr 12, 2024 · Understanding and analyzing MAUDE data helps us meet compliance obligations and serve a greater purpose: safeguarding patient health and optimizing device performance. In this article, we will discuss best practices for MAUDE data utilization and constraints to keep in mind during analysis.

8. www.accessdata.fda.gov › scripts › cdrhMAUDE User Instructions - Food and Drug Administration

   www.accessdata.fda.gov › scripts › cdrh

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   How is the MAUDE Database Full Text Search Index searched? Because of the amount of MAUDE data, you must select the 2-year period in which to search. Your search term can be the exact name of a...

9. www.nectarpd.com › maude-databaseThe Maude Database: A Comprehensive Guide for Medical...

   www.nectarpd.com › maude-database

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   The Maude Database, short for Manufacturer and User Facility Device Experience, is a publicly accessible database maintained by the U.S. Food and Drug Administration (FDA). It serves as a repository for reports of adverse events and product problems associated with medical devices.

10. www.ecri.org › components › MaudeFDA Device Reports - ECRI

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    Search FDA's Manufacturer and User Facility Device Experience (MAUDE) database. Already a Member? Log in Here. Overview. Our search engine for the MAUDE database allows users to apply search criteria such as device type, catalog number, and lot number.