8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
STUARTS TRANSPORT MEDIUM
FDA 510(k)
FDA Class 1
·Microbiology
DYNAREX/TILLOTSON NON-STERILE POWDER FREE BLUE NITRILE PATIENT EXAM GLOVE FOR USE WITH CHEMOTHERAPY DRUGS
FDA 510(k)
FDA Class 1
·General Hospital
BKS Revision Sleeves System
FDA 510(k)
FDA Class 2
·Orthopedic
PROMUS PREMIER?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 18, 2014
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·W.L. GORE & ASSOCIATES·Product code MIH·October 20, 2010
LENSX LASER SYSTEM
FDA Adverse Event
Injury
·ALCON - LENSX LASERS, INC.·Product code OOE·December 17, 2012
STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·June 22, 2017
STARDRIVE SCRWDRVR SHFT/T4 50MM/SELF-RETAINING/HXC
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·April 26, 2017