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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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182 records meeting your search criteria returned- Product Code: CBK Product Problem: Premature Discharge of Battery Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
RESPIRONICS, INC TRILOGY 100 06/28/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
GE IVENT 05/26/2016
NEWPORT MEDICAL INSTRUMENTS, INC HT50 VENTILATOR 04/25/2016
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