3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BATTERY 14.8V, 6.3 AH LI-ION BATTERY
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 21, 2014
VIPER 2 TORQUE DRIVER SHAFT
FDA Adverse Event
Malfunction
·DEPUY SPINE, INC.·Product code HXX·October 11, 2010
SPECTRANETICS LEAD LOCKING DEVICE
FDA Adverse Event
Injury
·SPECTRANETICS CORPORATION.·Product code DRB·December 20, 2012