4 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OLYMPUS THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code GEI·May 7, 2015
LIFESTAR VASCULAR STENT SYSTEM
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·May 27, 2014
COOL-TIP RF ELECTRODE
FDA Adverse Event
Malfunction
·COVIDIEN VALLEYLAB·Product code GEI·October 19, 2010
PROPLEGE CORONARY SINUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DWF·January 11, 2013