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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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105 records meeting your search criteria returned- Product Code: DRM Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL, INC. - 3015876 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 01/04/2023
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 10/16/2022
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 10/16/2022
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 07/12/2022
PHYSIO-CONTROL, INC. - 3015876 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 05/07/2022
PHYSIO-CONTROL, INC. - 3015876 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 04/13/2022
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 04/13/2022
ZOLL CIRCULATION AUTOPULSE® PLATFORM RESUSCITATION 01/05/2022
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 11/10/2021
JOLIFE AB - 3005445717 LUCAS 2, 2.1 SW, IN SHIPPING BOX, EN 09/09/2021
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