9 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SIMILAR DEVICE BNI75TCDDH, PMA # P030031
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2017
SIMILAR DEVICE DI7TCBLRT, PMA # P030031
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 9, 2015
NV MICROCATHETER
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·July 9, 2020
BARD TEGRESS URETHRAL BULKING AGENT
FDA Adverse Event
Injury
·C.R. BARD, INC.·Product code LNM·December 27, 2006
MEDTRONIC NAVIGATION
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·March 1, 2024
7.0MM TI SIDE-OPENING SCREW 50MM
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code MNH·April 2, 2013
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·March 25, 2011
E.S. UNIT, POWER CONTROL
FDA Adverse Event
Injury
·COVIDIEN LP (VALLEYLAB)·Product code GEI·April 14, 2008
THERMOCOOL® SMART TOUCH¿ BI-DIRECTIONAL NAVIGATION CATHETER P030031/S053
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC.·Product code LPB·April 18, 2018