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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience(MAUDE)
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10 records meeting your search criteria returned- Product Code: DTK Product Problem: Device Markings/Labelling Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. DENALI JUGULAR SYSTEM 03/08/2021
CORDIS CORPORATION 466FXXXX 05/05/2017
CORDIS CORPORATION OPTEASE RETRIEVABLE VENA CAVA FILTER - 5 03/11/2016
CORDIS CORPORATION OPTEASE RETRIEVABLE VENA CAVA FILTER - 5 09/02/2015
WILLIAM COOK EUROPE UNKNOWN 07/31/2015
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 06/24/2015
CORDIS CORPORATION OPTEASE RETRIEVABLE VENA CAVA FILTER - 5 01/23/2015
CORDIS DE MEXICO OPTEASE RETRIEVABLE VENA CAVA FILTER - 5 08/14/2014
CORDIS DE MEXICO OPTEASE RETRIEVABLE VENA CAVA FILTER - 5 08/13/2014
CORDIS DE MEXICO OPTEASE RETRIEVABLE VENA CAVA FILTER - 5 07/03/2014
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