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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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127 records meeting your search criteria returned- Product Code: FJS Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
UNKNOWN PD CATHETER 08/09/2023
UNKNOWN PD CATHETER 08/09/2023
UNKNOWN PD CATHETER 08/09/2023
COVIDIEN MFG SOLUTIONS S.A. ARGYLE 08/07/2023
COVIDIEN MFG SOLUTIONS S.A. ARGYLE 07/26/2023
Unknown Manufacturer PD (PERITONEAL DIALYSIS) CATHETER 07/18/2023
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL CATHETER 04/05/2023
COVIDIEN LP LLC NORTH HAVEN DIALYSIS UNKNOWN 03/08/2023
COVIDIEN MFG SOLUTIONS S.A. DIALYSIS UNKNOWN 11/15/2022
COVIDIEN MFG SOLUTIONS S.A. DIALYSIS UNKNOWN 11/14/2022
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