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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
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90 records meeting your search criteria returned- Product Code: NIO Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 08/27/2014
BOSTON SCIENTIFIC - MAPLE GROVE EPIC? VASCULAR 08/14/2014
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTAR VASCULAR STENT SYSTEM 07/16/2014
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 05/06/2014
BOSTON SCIENTIFIC - MAPLE GROVE EPIC? VASCULAR 04/16/2014
BOSTON SCIENTIFIC BOSTON SCIENTIFIC 03/26/2014
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 03/10/2014
MEDTRONIC IRELAND ASSURANT COBALT 02/28/2014
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 01/31/2014
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 01/07/2014
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