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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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330 records meeting your search criteria returned- Product Code: GEI Product Problem: Defective Device Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
COVIDIEN LP LIGASURE 12/15/2022
BOSTON SCIENTIFIC CORPORATION REZUM 12/12/2022
COVIDIEN MFG DC BOULDER FORCE FX 12/08/2022
STRYKER INSTRUMENTS NEPTUNE E-SEP 12/07/2022
BOSTON SCIENTIFIC CORPORATION RF3000 RADIOFREQUENCY GENERATOR 11/30/2022
COVIDIEN LP LIGASURE ATLAS 11/21/2022
COVIDIEN LIGASURE MARYLAND JAW 11/15/2022
OLYMPUS CORPORATION OF THE AMERICAS THUNDERBEAT 11/04/2022
OLYMPUS WINTER & IBE GMBH CELONPROBREATH (5 PCS) 10/25/2022
OLYMPUS WINTER & IBE GMBH CELONPROBREATH (5 PCS) 10/25/2022
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