8 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TUFF UNICON IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 5, 2025
TUFF UNICON IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 5, 2025
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 3, 2025
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR INC.·Product code MGB·October 12, 2010
EMBOSHIELD NAV6 EMBOLIC PROTECTION SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NTE·October 12, 2010
EEA 21MM SINGLE USE STAPLER WITH 3.5MM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY USSC·Product code GDW·March 6, 2013
ULTRAFLEX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code ESW·February 25, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC·Product code JAA·February 22, 2008