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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
MEDTRONIC EUROPE SARL EVERA MRI S VR SURESCAN 01/03/2024
MEDTRONIC EUROPE SARL IMPLANTABLE CARDIOVERTER DEFIBRILLATOR ( 01/02/2024
MEDTRONIC EUROPE SARL EVERA MRI XT DR SURESCAN 01/02/2024
MEDTRONIC EUROPE SARL EVERA MRI XT DR SURESCAN 12/27/2023
MEDTRONIC EUROPE SARL VISIA AF S VR 12/27/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT DR SURESCAN 12/22/2023
MEDTRONIC EUROPE SARL AURORA EV-ICD¿ MRI SURESCAN¿ 12/22/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT DR SURESCAN 12/21/2023
MEDTRONIC EUROPE SARL EVERA MRI XT DR SURESCAN 12/21/2023
MEDTRONIC EUROPE SARL COBALT¿ XT DR MRI SURESCAN¿ 12/19/2023
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