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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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8 records meeting your search criteria returned- Product Code: NTE Patient Problem: Hemorrhage, Cerebral Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
INVATEC SPA MO.MA ULTRA 03/04/2019
COVIDIEN SPIDER FX 03/04/2019
BOSTON SCIENTIFIC CORPORATION FILTERWIRE EZ 11/09/2018
INVATEC SPA MO.MA ULTRA 07/13/2018
COVIDIEN SPIDER FX 07/13/2018
INVATEC SPA MO.MA 6F ID 05/18/2017
COVIDIEN SPIDER FX 02/14/2017
INVATEC SPA MO.MA ULTRA 02/14/2017
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