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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
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8 records meeting your search criteria returned- Product Code: DWF Product Problem: Device Packaging Compromised Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SURGE CARDIOVASCULAR ANTEGRADE CARDIOPLEGIA CANNULA 05/16/2018
DATASCOPE CORP. CUSTOM PERFUSION PACK 12/16/2014
DATASCOPE CORP CUSTOM PERFUSION PACK 12/16/2014
EDWARDS LIFESCIENCES AORTIC ROOT CANNULA 03/18/2014
DATASCOPE CORP., 4 TO 1 PLEGIOX SET 03/05/2014
DATASCOPE CORP. 4 TO 1 PLEGIOX SET 03/05/2014
DATASCOPE CORP. 4 TO 1 PLEGIOX SET 03/05/2014
EDWARDS LIFESCIENCES EZ GLIDE AORTIC DEVICE 01/02/2014
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