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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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
MPRI CAPSURE SP 03/15/2019
MPRI CAPSUREFIX NOVUS 03/12/2019
MPRI CAPSUREFIX NOVUS 03/01/2019
MPRI CAPSUREFIX NOVUS 02/28/2019
MPRI MYOCARDIAL LEAD 01/29/2019
BOSTON SCIENTIFIC CORPORATION FINELINE II STEROX 01/28/2019
MPRI CAPSUREFIX NOVUS 01/24/2019
BOSTON SCIENTIFIC CORPORATION PERMANENT PACEMAKER ELECTRODE 01/22/2019
BOSTON SCIENTIFIC CORPORATION FINELINE II EZ STEROX 01/15/2019
MEDTRONIC SINGAPORE OPERATIONS CAPSUREFIX NOVUS 01/09/2019
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