53 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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FORTIFY ASSURA VR ICD_IDE_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017
COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·June 15, 2006
ELLIPSE VR ICD
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·March 29, 2017
COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·June 15, 2006
CD2257-40Q FORTIFY ASSURA DR ICD_IDE_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·June 14, 2017
FORTIFY ASSURA VR ICD_IDE_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code NVZ·October 31, 2017
COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·June 21, 2006
DELTA CER HEAD 12/14 36MM +1.5
FDA Adverse Event
Injury
·8010379 DEPUY INTL., LTD.·Product code LZO·March 5, 2013
ATTAIN OTW
FDA Adverse Event
Injury
·MPRI·Product code LWP·August 7, 2014
FORTIFY ST DR, U1.6 SJ4 ID
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.·Product code LWS·January 18, 2017
FORTIFYASSURA DR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 3, 2017
FORTIFY ASSURA VR ICD_O_US
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·January 27, 2016
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 17, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·November 10, 2014
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·July 20, 2015
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 5, 2015