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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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9 records meeting your search criteria returned- Product Code: LIT Patient Problem: Rupture Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
CORDIS CORPORATION POWERFLEXPRO 6MM10CM 80 03/22/2022
MEDTRONIC MEXICO ADMIRAL XTREME 09/17/2021
MEDTRONIC MEXICO ADMIRAL XTREME 07/06/2021
BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE RX PTA DILATATION CATHETER 07/01/2021
BARD PERIPHERAL VASCULAR, INC. VACCESS PTA DILATATION CATHETER 05/06/2020
COVIDIEN EVERCROSS 035 11/15/2019
MEDTRONIC MEXICO PACIFIC PLUS 07/08/2019
KANEKA CORPORATION SHIDEN HP 06/04/2019
CORDIS CASHEL UNKSAVVY 02/12/2019
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