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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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205 records meeting your search criteria returned- Product Code: FJK Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
NIPRO (THAILAND) CORP. LTD. NIPRO BLOOD TUBING SET W/TP 02/27/2024
NIPRO (THAILAND) CORP. LTD. NIPRO BLOOD TUBING SET W/TP 02/27/2024
NOVAMED (ANTALYA) MULTIFILTRATEPRO SECUCAS CI-CA HD 02/26/2024
B. BRAUN MEDICAL INC. HEMODIALYSIS BLOODLINES 02/06/2024
ST. WENDEL AG ULTRAFLUX EMIC2 07/14/2023
NOVAMED (ANTALYA) MULTIFILTRATEPRO SECUCAS CI-CA HD 05/26/2023
ERIKA DE REYNOSA, S.A. DE C.V. FMC BLOODLINE 04/21/2023
ERIKA DE REYNOSA, S.A. DE C.V. FMC BLOODLINE 04/21/2023
ERIKA DE REYNOSA, S.A. DE C.V. FMC BLOODLINE 02/24/2023
ERIKA DE REYNOSA, S.A. DE C.V. FMC BLOODLINE 02/24/2023
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