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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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
ST. JUDE MEDICAL - NEUROMODULATION (PUER OCTRODE TRIAL LEAD KIT, 60CM LENGTH 08/09/2023
ABBOTT MEDICAL OCTRODE LEAD KIT, 60CM LENGTH 08/07/2023
ST. JUDE MEDICAL - NEUROMODULATION (PUER OCTRODE LEAD KIT, 60CM LENGTH 08/03/2023
ST. JUDE MEDICAL - NEUROMODULATION (PUER OCTRODE LEAD KIT, 60CM LENGTH 08/03/2023
ABBOTT MEDICAL PENTA 3MM LEAD, 60 CM 08/01/2023
ST. JUDE MEDICAL - NEUROMODULATION (PUER OCTRODE LEAD KIT, 60CM LENGTH 07/27/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. INTELLIS 07/26/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. INTELLIS 07/25/2023
ABBOTT MEDICAL PENTA 3MM LEAD, 60 CM 07/24/2023
ABBOTT MEDICAL PENTA 3MM LEAD, 60 CM 07/20/2023
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