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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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13 records meeting your search criteria returned- Product Code: NIQ Product Problem: Failure To Adhere Or Bond Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
CORDIS CORPORATION UNKNOWN CYPHER JAPAN 04/16/2018
CORDIS CASHEL UNKNOWN CYPHER JAPAN 12/01/2017
CORDIS DE MEXICO UNKNOWN CYPHER JAPAN 03/16/2017
CORDIS DE MEXICO UNKSTENT 10/14/2016
CORDIS CORPORATION CYPHER SIROLIMUS-ELUTING CORONARY STENT 08/28/2015
CORDIS CORPORATION CYPHER SIROLIMUS-ELUTING CORONARY STENT 08/28/2015
CORDIS CORPORATION CYPHER SIROLIMUS-ELUTING CORONARY STENT 07/21/2015
CORDIS CORPORATION CYPHER SIROLIMUS-ELUTING CORONARY STENT 04/27/2015
CORDIS DE MEXICO CYPHER SIROLIMUS-ELUTING CORONARY STENT 06/25/2014
CORDIS DE MEXICO CYPHER SIROLIMUS-ELUTING CORONARY STENT 05/01/2014
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