Data from: MAUDE (Manufacturer and User Facility Device Experience)
- healthdata.gov
- data.virginia.gov
- +4more
application/rdfxml +5Updated Feb 25, 2021
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EmailClick to copy linkLink copiedCiteopen.fda.gov (2021). MAUDE (Manufacturer and User Facility Device Experience) [Dataset]. https://healthdata.gov/dataset/MAUDE-Manufacturer-and-User-Facility-Device-Experi/u4i2-5xvtcsv, application/rssxml, json, tsv, application/rdfxml, xmlAvailable download formatsDataset updatedFeb 25, 2021Dataset provided byopen.fda.govDescriptionMAUDE 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.
MAUDE with Patient Involvement
- johnsnowlabs.com
csvUpdated Jan 20, 2021ShareFacebookTwitterEmailClick to copy linkLink copiedCiteJohn Snow Labs (2021). MAUDE with Patient Involvement [Dataset]. https://www.johnsnowlabs.com/marketplace/maude-with-patient-involvement/csvAvailable download formatsDataset updatedJan 20, 2021Dataset authored and provided byJohn Snow LabsArea coveredUnited StatesDescriptionMAUDE (Manufacturer and User Facility Device Experience) dataset represents reports of adverse events involving medical devices the data consist of voluntary Reports since June 1993, User facility Reports since 1991, Distributor Reports since 1993, and Manufacturer Reports since August 1996.
Manufacturer And User Facility Device Experience Database
- johnsnowlabs.com
csvUpdated Jan 20, 2021ShareFacebookTwitterEmailClick to copy linkLink copiedCiteJohn Snow Labs (2021). Manufacturer And User Facility Device Experience Database [Dataset]. https://www.johnsnowlabs.com/marketplace/manufacturer-and-user-facility-device-experience-database/csvAvailable download formatsDataset updatedJan 20, 2021Dataset authored and provided byJohn Snow LabsArea coveredUnited StatesDescriptionMAUDE data represents Reports of adverse Events involving medical Devices the datasets consist of voluntary Reports since June 1993, User facility Reports since 1991, Distributor Reports since 1993, and Manufacturer Reports since August 1996.
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FacebookTwitterEmailMAUDE 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.