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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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267 records meeting your search criteria returned- Product Code: DWF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
MEDTRONIC MEXICO CUSTOM PACK 01/05/2021
PERFUSION SYSTEMS RCSP RETROGRADE CANNULA 12/15/2020
PERFUSION SYSTEMS DLP SILICONE RCSP RETROGRADE RETROGRADE 12/09/2020
PERFUSION SYSTEMS DLP SILICONE RCSP RETROGRADE RETROGRADE 12/08/2020
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 11/12/2020
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 11/03/2020
PERFUSION SYSTEMS BIO-MEDICUS NG 23 FR ARTERIAL CANNULA 10/21/2020
PERFUSION SYSTEMS BIO-MEDICUS NG 15 FR ARTERIAL CANNULA 10/21/2020
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 10/09/2020
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 09/23/2020
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