3 results
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30ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SPECTRANETICS GLIDELIGHT LASER SHEATH
FDA Adverse Event
Injury
·SPECTRANETICS CORPORATION·Product code MFA·June 13, 2014
ARDIS PEEK IMPLANT 08X09X22
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code MAX·October 11, 2010
WANDA¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code LIT·December 13, 2012