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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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3 records meeting your search criteria returned- Product Code: OEV Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
RESOURCE OPTIMIZATION & INNOVATION, L.L. REGARD DEFIBRILLATOR PAD 10/30/2018
CAREFUSION/BD RESUS, INF W/MASK, RESV BAG, P/O, 6/CS 03/13/2017
CAREFUSION/BD RESUS,ADLT W/MSK,LRG TBG, P/O, 6/CS 03/09/2017
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