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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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20 records meeting your search criteria returned- Product Code: PGT Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
MINERVA SURGICAL, INC. SYMPHION RD- RESECTING DEVICE 3.6 10/26/2021
MINERVA SURGICAL, INC. SYMPHION RD- RESECTING DEVICE 3.6 09/23/2021
BOSTON SCIENTIFIC CORPORATION SYMPHION 05/23/2019
BOSTON SCIENTIFIC CORPORATION SYMPHION 05/03/2019
BOSTON SCIENTIFIC CORPORATION SYMPHION 03/28/2019
BOSTON SCIENTIFIC CORPORATION SYMPHION 02/07/2019
BOSTON SCIENTIFIC - MARLBOROUGH SYMPHION¿ TISSUE REMOVAL SYSTEM RESECTIN 06/20/2018
BOSTON SCIENTIFIC - MARLBOROUGH SYMPHION¿ TISSUE REMOVAL SYSTEM RESECTIN 04/25/2018
BOSTON SCIENTIFIC - MARLBOROUGH SYMPHION¿ TISSUE REMOVAL SYSTEM RESECTIN 03/16/2018
BOSTON SCIENTIFIC - MARLBOROUGH SYMPHION¿ TISSUE REMOVAL SYSTEM RESECTIN 01/02/2018
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