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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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226 records meeting your search criteria returned- Product Code: NIO Patient Problem: No Patient Involvement Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 05/16/2018
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 05/16/2018
BOSTON SCIENTIFIC - GALWAY EXPRESS® LD ILIAC / BILIARY 05/15/2018
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 04/11/2018
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 02/16/2018
BOSTON SCIENTIFIC - GALWAY EXPRESS® LD ILIAC / BILIARY 01/30/2018
BOSTON SCIENTIFIC - GALWAY EXPRESS® LD ILIAC / BILIARY 01/17/2018
AV-TEMECULA-CT ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 11/27/2017
AV-TEMECULA-CT OMNILINK ELITE PERIPHERAL STENT SYSTEM 11/21/2017
BOSTON SCIENTIFIC - GALWAY EPIC¿ VASCULAR 11/20/2017
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