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U.S. Department of Health and Human Services

MDR Database Search

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Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards | Inspections
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

Search MDR Database
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MDR Search Values
Product Description
 (mm/dd/yyyy)  use calendar to select date  use calendar to select date
     
 
Manufacturer and User Facility Device Experience Search: (for incidents after July 31, 1996)
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