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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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17 records meeting your search criteria returned- Product Code: DTE Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDTRONIC, INC. EXTERNAL TEMPORARY PACEMAKER / IMPLANT T 11/08/2023
MEDTRONIC, INC. DUAL CHAMBER TEMPORARY PACEMAKER 11/01/2022
MEDTRONIC, INC. DUAL CHAMBER TEMPORARY PACEMAKER 11/01/2022
MEDTRONIC, INC. MEDTRONIC EPG 10/06/2022
MEDTRONIC, INC. MEDTRONIC CABLE 09/26/2022
MEDTRONIC, INC. MEDTRONIC CABLE 09/24/2022
MEDTRONIC, INC. DUAL CHAMBER TEMPORARY PACEMAKER 09/24/2022
MEDTRONIC, INC. MEDTRONIC LEAD 08/12/2022
OSYPKA MEDICAL GMBH OSYPKA PACE 203H 06/08/2022
MEDTRONIC IRELAND MEDTRONIC LEAD 10/10/2021
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