4 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
1933149-1997-00005
FDA Adverse Event
Injury
·PURITAN-BENNETT CORP/SLEEP THERAPEUTICS DIVISION·Product code BZA·November 12, 1997
COBAS 8000 C702 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CFR·January 29, 2013
SM304 M-SERIES W/ZOOM
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIVISION·Product code INK·December 13, 2010
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 14, 2014