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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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6 records meeting your search criteria returned- Product Code: LJT Product Problem: Use of Device Problem Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
BARD ACCESS SYSTEMS, INC. PORT-A-CATH 04/19/2023
BARD ACCESS SYSTEMS, INC. BARDPORT, SLIMPORT, X-PORT 04/05/2023
ANGIODYNAMICS, INC. SMART PORT 08/17/2021
BARD ACCESS SYSTEMS, INC. POWERPORT 03/11/2021
ANGIODYNAMICS SMART PORT 03/09/2020
BARD ACCESS SYSTEMS POWERPORT MRI ISP, 8 FR CHRONOFLEX, SUTU 01/16/2020
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