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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
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9 records meeting your search criteria returned- Product Code: DRM Patient Problem: Rupture Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
JOLIFE AB - 3005445717 LUCAS 3 CHEST COMPRESSION SYSTEM 06/28/2023
PHYSIO-CONTROL, INC. - 3015876 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 01/04/2023
ZOLL CIRCULATION AUTOPULSE® PLATFORM RESUSCITATION 01/05/2022
PHYSIO-CONTROL, INC. - 3015876 LUCAS CHEST COMPRESSION SYSTEM 12/01/2018
PHYSIO-CONTROL LUCAS 10/29/2018
JOLIFE AB LUCAS(T) CPR CHEST COMPRESSION SYSTEM 09/09/2015
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 07/22/2014
JOLIFE AB LUCAS (T) CPR CHEST COMPRESSION SYSTEM 07/01/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 02/10/2014
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