327 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·VISTAKON (LENEFILCON A) SOFT (HYDROPHILIC) CONTACT LENS, CLEAR AND VISIBILITY TINTED WITH UV BLOCKER
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·LENEFILCON A HYDROPHILIC CONTACT LENSES
Richardson Retractor
FDA UDI
KOROS U.S.A., INC.·10840199542397·Richardson Retractor 3/4" Wide, 2" Deep
247
FDA UDI
SUNTECH MEDICAL, INC.·10840935105671·
MILLENNIUM MLC -120
FDA 510(k)
FDA Class 2
·Radiology
Catheter, Electrode Recording, Or Probe, Electrode Recording
FDA Pre-Market Approval
FDA Class 2
·NAVI-STAR DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER
Barrier, Absorbable, Adhesion
FDA Pre-Market Approval
FDA Class 3
·INTERGEL ADHESION PREVENTION SOLUTION
PROMUS ELEMENT ¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 5, 2013
ENRHYTHM DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·February 15, 2011
ADVISA DR MRI SURESCAN
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code NVZ·August 7, 2014
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
Death
·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 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
SIMILAR DEVICE NS7TCBL174HS, PMA # P990025
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·March 4, 2015