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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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17 records meeting your search criteria returned- Product Code: DRT Product Problem: Loss of Power Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL PHYSIO-CONTROL LP15 MONITOR 03/07/2017
ZOLL MEDICAL CORPORATION X SERIES 11/10/2016
WELCH ALLYN PROPAQ CS 246 07/28/2016
WELCH ALLYN PROPAQ ENCORE 02/25/2016
WELCH ALLYN PROPAQ CS 242 01/12/2016
WELCH ALLYN PROPAQ LT 802 10/08/2015
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 09/28/2015
WELCH ALLYN PROPAQ ENCORE 206/EL 09/09/2015
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 09/04/2015
WELCH ALLYN PROPAQ CS 244 08/27/2015
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