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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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47 records meeting your search criteria returned- Product Code: KDI Product Problem: Reflux within Device Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 07/13/2022
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 06/28/2022
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 05/31/2022
CONCORD MANUFACTURING 2008K OLC ONLY WITH HEPARIN PUMP 05/09/2022
CONCORD MANUFACTURING 2008K OLC ONLY WITH HEPARIN PUMP 04/04/2022
CONCORD MANUFACTURING 2008T HD SYS. W/O CDX BLUE STAR 03/24/2022
CONCORD MANUFACTURING 2008K HEMODIALYSIS SYS. OLC/DIASAFE PLUS 08/30/2021
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 08/27/2021
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYS., WITH CDX 07/22/2021
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 06/16/2021
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