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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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61 records meeting your search criteria returned- Product Code: DRM Product Problem: Loss of Power Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
MICHIGAN INSTRUMENTS, INC LIFE-STAT 03/13/2018
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 02/21/2018
PHYSIO-CONTROL, INC./PHYSIO-CONTROL MANU LUCAS 10/21/2016
PHYSIO-CONTROL, INC./PHYSIO-CONTROL MANU LUCAS II 09/19/2016
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 06/23/2016
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 06/03/2016
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 06/03/2016
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 06/03/2016
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/05/2015
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 07/13/2015
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