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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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95 records meeting your search criteria returned- Product Code: NEU Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
HOLOGIC, INC LOCALIZER 07/26/2022
BARD PERIPHERAL VASCULAR, INC. SENOMARK 05/20/2022
BARD PERIPHERAL VASCULAR, INC. SENOMARK 05/19/2022
HOLOGIC, INC. BIOZORB 05/11/2022
HOLOGIC, INC. TRIMARK 05/11/2022
Unknown Manufacturer INTER-SCATTER BACKSCATTER 04/18/2022
BARD PERIPHERAL VASCULAR, INC. ULTRACLIP DUAL TRIGGER 04/07/2022
HOLOGIC, INC. TRIMARK EVIVA 03/24/2022
HOLOGIC, INC. BIOZORB 03/15/2022
COVIDIEN LP BARRX UNKNOWN BEACON NEEDLE 03/07/2022
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