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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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11 records meeting your search criteria returned- Product Code: DRT Product Problem: Device Inoperable Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS NA 08/01/2017
NIHON KOHDEN CORPORATION ZM-520PA 10/21/2016
NIHON KOHDEN TOMIOKA CORPORATION ZM-540PA 04/01/2016
NIHON KOHDEN TOMIOKA CORPORATION ZM-541PA 03/18/2016
NIHON KOHDEN TOMIOKA CORPORATION ZM-520PA 02/18/2016
NIHON KOHDEN CORPORATION ZM-541PA 02/11/2016
NIHON KOHDEN CORPORATION ZM-521PA 02/06/2016
NIHON KOHDEN TOMIOKA CORPORATION ZM-520PA 01/07/2016
NIHON KOHDEN TOMIOKA CORPORATION ZM-541PA 12/24/2015
NIHON KOHDEN TOMIOKA CORPORATION ZM-530PA 12/19/2015
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