MAUDE (Manufacturer and User Facility Device Experience).

Dataset Identification:

Resource Abstract:
description: <p>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.</p>; abstract: <p>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.</p>
Citation
Title MAUDE (Manufacturer and User Facility Device Experience).
creation  Date   2018-06-09T14:17:38.795365
Resource language: 
Processing environment:  
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Resource distribution information

Digital Transfer Options
Linkage for online resource
name Dublin Core references URL
URL: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM
protocol WWW:LINK-1.0-http--link
link function information
Description URL provided in Dublin Core references element.

Metadata data stamp:  2018-08-06T19:59:32Z
Resource Maintenance Information
maintenance or update frequency: 
notes: This metadata record was generated by an xslt transformation from a dc metadata record; Transform by Stephen M. Richard, based on a transform by Damian Ulbricht. Run on 2018-08-06T19:59:32Z
Metadata contact - pointOfContact
organisation Name  CINERGI Metadata catalog
Contact information
Address
electronic Mail Address cinergi@sdsc.edu
Metadata language  eng
Metadata character set encoding:   utf8
Metadata standard for this record:  ISO 19139 Geographic Information - Metadata - Implementation Specification
standard version:  2007
Metadata record identifier:  urn:dciso:metadataabout:6ac8b4d0-ca86-4be8-b841-5f148b58a45b

Metadata record format is ISO19139 XML (MD_Metadata)