4 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
TUFF PRO IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 31, 2025
TUFF PRO IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 31, 2025
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·March 12, 2013
4.2MM THREE-FLUTED DRILL BIT QC/330MM/100MM CALIBRATION
FDA Adverse Event
Injury
·SYNTHES BETTLACH·Product code HTW·January 3, 2017