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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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11 records meeting your search criteria returned- Product Code: FAD Product Problem: Bent Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC - COSTA RICA (COYOL) POLARIS¿ ULTRA 04/20/2018
BOSTON SCIENTIFIC - COSTA RICA (COYOL) MODIFICATION TO CONTOUR POLARIS URETERAL 03/22/2018
BOSTON SCIENTIFIC - COSTA RICA (COYOL) MODIFICATION TO CONTOUR POLARIS URETERAL 03/22/2018
BOSTON SCIENTIFIC - COSTA RICA (COYOL) POLARIS¿ ULTRA 03/22/2018
BOSTON SCIENTIFIC - COSTA RICA (COYOL) POLARIS¿ ULTRA 03/22/2018
BOSTON SCIENTIFIC - COSTA RICA (COYOL) SUREDRIVE TM 12/12/2017
BOSTON SCIENTIFIC - COSTA RICA (COYOL) SUREDRIVE TM 12/11/2017
BOSTON SCIENTIFIC - COSTA RICA (COYOL) SUREDRIVE TM 12/11/2017
BOSTON SCIENTIFIC - COSTA RICA (COYOL) EXPEL¿ NEPHROURETERAL STENT SYSTEM WITH 06/01/2017
BOSTON SCIENTIFIC - COSTA RICA (COYOL) PERCUFLEX¿ NEPHROURETERAL STENT 07/24/2015
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