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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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91 records meeting your search criteria returned- Product Code: NIQ Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2015
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ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND RESOLUTE ONYX RX 05/12/2020
MEDTRONIC IRELAND RESOLUTE ONYX RX 01/30/2020
MEDTRONIC IRELAND RESOLUTE ONYX OTW 01/27/2020
MEDTRONIC IRELAND RESOLUTE ONYX RX 07/18/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 07/12/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 07/01/2019
MEDTRONIC IRELAND ENDEAVOR RX 05/07/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 03/06/2019
BOSTON SCIENTIFIC CORPORATION SYNERGY 02/05/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/17/2018
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