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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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56 records meeting your search criteria returned- Product Code: DRG Product Problem: Device Inoperable Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
NKUS LAB CENTRAL MONITORING SYSTEM 02/07/2018
NIHON KOHDEN CORPORATION ORG-9110A 08/17/2017
NKUS LAB CENTRAL MONITORING SYSTEM 02/15/2017
NKUS LAB CENTRAL MONITORING SYSTEM 02/15/2017
NKUS LAB CENTRAL MONITORING SYSTEM 02/08/2017
NKUS LAB CENTRAL MONITORING SYSTEM 01/27/2017
NIHON KOHDEN TOMIOKA CORPORATION ORG-9100A 09/11/2016
PHILIPS MEDICAL SYSTEMS INTELLIVUE 08/22/2016
NKUS LAB CENTRAL MONITORING SYSTEM 08/12/2016
NIHON KOHDEN CORPORATION ORG-9100A 08/07/2016
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