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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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162 records meeting your search criteria returned- Product Code: LDD Product Problem: Device Inoperable Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS CODEMASTER XE 04/03/2018
PHILIPS MEDICAL SYSTEMS 3 LEAD IEC ECG PATIENT CABLE 12/15/2016
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 12/08/2016
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 05/09/2016
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 03/25/2016
PHILIPS MEDICAL SYSTEMS LARGE SWITCHLESS INTERNAL PADDLES 02/26/2016
PHILIPS MEDICAL SYSTEMS CODEMASTER XE 02/02/2016
PHILIPS MEDICAL SYSTEMS CODEMASTER XL+ 11/06/2015
PHILIPS MEDICAL SYSTEMS SMALL SWITCHED INT PDLS 10/12/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER XL+ 01/20/2015
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