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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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

 
 
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
US SURGICAL PUERTO RICO ENDO GIA ULTRA 07/05/2018
US SURGICAL PUERTO RICO EEA 07/05/2018
COVIDIEN LP LLC NORTH HAVEN RELIATACK 07/03/2018
US SURGICAL PUERTO RICO EEA 07/03/2018
US SURGICAL PUERTO RICO ILA 07/03/2018
US SURGICAL PUERTO RICO ILA 07/03/2018
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 07/02/2018
US SURGICAL PUERTO RICO ENDO GIA ULTRA 07/02/2018
COVIDIEN LP LLC NORTH HAVEN RELIATACK 06/29/2018
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 06/29/2018
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