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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 VISIA AF MRI XT VR SURESCAN 07/26/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA¿ XT DR 07/26/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA¿ XT DR 07/25/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA¿ XT DR 07/20/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT DR SURESCAN 07/20/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI XT DR SURESCAN 07/20/2023
MEDTRONIC EUROPE SARL EVERA MRI XT DR SURESCAN 07/18/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. EVERA MRI S DR SURESCAN 07/18/2023
MEDTRONIC EUROPE SARL EVERA MRI XT DR SURESCAN 07/17/2023
MEDTRONIC EUROPE SARL EVERA¿ XT DR 07/14/2023
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