3 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OPTIFLUX F250NRE DIALYZER
FDA Adverse Event
Malfunction
·OGDEN MANUFACTURING·Product code KDI·May 19, 2014
CARDIOVASCULAR PROCEDURE KIT
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·November 5, 2010
SERIES 20000 LEGACY
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOLGY CENTER·Product code HQC·December 20, 2012