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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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292 records meeting your search criteria returned- Product Code: NRY Product Problem: Device Damaged Prior to Use Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 06/21/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 06/20/2019
PENUMBRA, INC. PENUMBRA SYSTEM JET7 REPERFUSION CATHETE 05/28/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 05/13/2019
PENUMBRA, INC. PENUMBRA SYSTEM JET 7 REPERFUSION CATHET 05/10/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 05/08/2019
PENUMBRA, INC. PENUMBRA SYSTEM JETD REPERFUSION CATHETE 05/08/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 05/01/2019
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 REPERFUSION CATHE 05/01/2019
PENUMBRA, INC. PENUMBRA SYSTEM JET7 REPERFUSION CATHETE 04/15/2019
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