2 datasets found
  1. Data from: MAUDE (Manufacturer and User Facility Device Experience)

    • healthdata.gov
    • cloud.csiss.gmu.edu
    • +5more
    application/rdfxml +5
    Updated Feb 25, 2021
    + more versions
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    open.fda.gov (2021). MAUDE (Manufacturer and User Facility Device Experience) [Dataset]. https://healthdata.gov/dataset/MAUDE-Manufacturer-and-User-Facility-Device-Experi/u4i2-5xvt
    Explore at:
    csv, application/rssxml, json, tsv, application/rdfxml, xmlAvailable download formats
    Dataset updated
    Feb 25, 2021
    Dataset provided by
    Food and Drug Administrationhttp://www.fda.gov/
    Description

    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.

  2. Maude Winston Importer/Buyer Data in USA, Maude Winston Imports Data

    • seair.co.in
    Updated Feb 18, 2024
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    Seair Exim (2024). Maude Winston Importer/Buyer Data in USA, Maude Winston Imports Data [Dataset]. https://www.seair.co.in
    Explore at:
    .bin, .xml, .csv, .xlsAvailable download formats
    Dataset updated
    Feb 18, 2024
    Dataset provided by
    Seair Exim Solutions
    Authors
    Seair Exim
    Area covered
    United States
    Description

    Subscribers can find out export and import data of 23 countries by HS code or product’s name. This demo is helpful for market analysis.

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Share
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TwitterTwitter
Email
Click to copy link
Link copied
Close
Cite
open.fda.gov (2021). MAUDE (Manufacturer and User Facility Device Experience) [Dataset]. https://healthdata.gov/dataset/MAUDE-Manufacturer-and-User-Facility-Device-Experi/u4i2-5xvt
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Data from: MAUDE (Manufacturer and User Facility Device Experience)

Related Article
Explore at:
csv, application/rssxml, json, tsv, application/rdfxml, xmlAvailable download formats
Dataset updated
Feb 25, 2021
Dataset provided by
Food and Drug Administrationhttp://www.fda.gov/
Description

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.

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