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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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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
JOLIFE AB - 3005445717 LUCAS 3 CHEST COMPRESSION SYSTEM 05/12/2021
JOLIFE AB - 3005445717 LUCAS 3 CHEST COMPRESSION SYSTEM 05/12/2021
PHYSIO-CONTROL, INC. - 3015876 LUCAS CPR CHEST COMPRESSION SYSTEM 02/01/2021
JOLIFE AB - 3005445717 LUCAS 2, 2.1 SW, IN SHIPPING BOX, EN 02/01/2021
ZOLL CIRCULATION AUTOPULSE PLATFORM RESUSCITATION 10/03/2020
PHYSIO-CONTROL, INC. - 3015876 UNKNOWN_MEDICAL - LUND_PRODUCT 07/01/2020
PHYSIO-CONTROL, INC. - 3015876 LUCAS CPR CHEST COMPRESSION SYSTEM 07/01/2020
PHYSIO-CONTROL, INC. - 3015876 LUCAS CPR CHEST COMPRESSION SYSTEM 04/21/2020
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 03/27/2020
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 03/26/2020
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