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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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78 records meeting your search criteria returned- Product Code: DQO Product Problem: Occlusion Within Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 04/24/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 04/21/2017
CORDIS CASHEL 466P306X 03/13/2017
CORDIS CORPORATION 466P306X 03/12/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 03/10/2017
CORDIS CORPORATION 466P306X 03/08/2017
CORDIS CASHEL TRAPEASE PVCF BRACH 90CM CSI 03/06/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 02/23/2017
CORDIS CASHEL TRAPEASE 02/17/2017
CORDIS CORPORATION TRAPEASE W/CSI INTRO KIT 55CM 10/20/2016
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