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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: DRO Product Problem: Device Sensing Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
COVIDIEN 1410Z KENDALL 1PR/PK 10PR/CA 09/28/2021
COVIDIEN ADULT MULTI-FUNCTION DEFIBRILLATION ELEC 11/15/2018
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 12/29/2015
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