MAUDE (Manufacturer and User Facility Device Experience)

Metadata Updated: November 10, 2020

MAUDE data represents reports of adverse events involving medical devices. The data consists of all voluntary reports since June, 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August, 1996.

Access & Use Information

Public: This dataset is intended for public access and use. License: See this page for license information.

Downloads & Resources

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Dates

Metadata Created Date	November 10, 2020
Metadata Updated Date	November 10, 2020

Metadata Source

Data.json Data.json Metadata
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Harvested from Healthdata.gov

Additional Metadata

Resource Type	Dataset
Metadata Created Date	November 10, 2020
Metadata Updated Date	November 10, 2020
Publisher	Department of Health & Human Services
Unique Identifier	Unknown
Maintainer	openFDA
Identifier	63ef68f9-a795-463d-9b62-48bccd13130f
Data First Published	2014-01-09
Data Last Modified	2016-09-02
Public Access Level	public
Bureau Code	009:10
Metadata Context	https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
Metadata Catalog ID	https://healthdata.gov/data.json
Schema Version	https://project-open-data.cio.gov/v1.1/schema
Catalog Describedby	https://project-open-data.cio.gov/v1.1/schema/catalog.json
Homepage URL	https://healthdata.gov/dataset/maude-manufacturer-and-user-facility-device-experience-0
License	https://opendatacommons.org/licenses/odbl/1.0/
Program Code	009:005
Source Datajson Identifier	True
Source Hash	9b2a57e30165781a7d464806dd5fabf22081ffcb
Source Schema Version	1.1

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