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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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8 records meeting your search criteria returned- Product Code: DWF Product Problem: Malposition of Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH AVALON ELITE DUAL LUMEN CATHETER 07/03/2023
MAQUET CARDIOPULMONARY GMBH AVALON ELITE DUAL LUMEN CATHETER 07/03/2023
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 11/14/2022
PERFUSION SYSTEMS EOPA ARTERIAL CANNULA 06/21/2021
ORIGEN BIOMEDICAL, INC. ORIGEN REINFORCED DUAL LUMEN CATHETER 03/13/2019
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 04/26/2017
CARDIACASSIST INC PROTEK DUO VENO-VENOUS CANNULA 05/13/2016
CARDIACASSIST INC PROTEK DUO 02/25/2016
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