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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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4 records meeting your search criteria returned- Product Code: FMF Patient Problem: Syncope/Fainting Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 12/14/2022
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 10/14/2021
NOVO NORDISK A/S, NOVOPEN 5 07/19/2021
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 04/05/2021
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