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aproimos

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aproimos

Re: None

Monday, 04/08/2013 6:05:27 PM

Monday, April 08, 2013 6:05:27 PM

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9-5-13: MAUDE - Manufacturer and User Facility Device Experience

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

http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM

Interesting reading.
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