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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
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5 records meeting your search criteria returned- Product Code: NIQ Product Problem: Device Slipped Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND RESULUTE ONYX STENT 03/23/2022
BIOTRONIK AG ORSIRO 01/29/2021
COVIDIEN LP STENT 02/04/2019
MEDINOL LTD. ELUNIR¿ RIDAFOROLIMUS ELUTING CORONARY S 07/01/2018
AV-TEMECULA-CT XIENCE PRIME SV EVEROLIMUS ELUTING CORON 06/13/2018
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