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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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224 records meeting your search criteria returned- Product Code: PDU Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CORDIS CORPORATION OUTBACK ELITE 120CM RE-ENTRY 09/29/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETERS 09/14/2020
CORDIS CORPORATION OUTBACK ELITE 120CM RE-ENTRY 08/07/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETER 07/20/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETERS 07/16/2020
C.R. BARD, INC. (GFO) CROSSER CTO RECANALIZATION CATHETERS 07/16/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETER 07/16/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETERS 07/14/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETER 07/14/2020
BARD PERIPHERAL VASCULAR, INC. CROSSER CTO RECANALIZATION CATHETERS 06/23/2020
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