6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Trivicta Hip Stem
FDA 510(k)
FDA Class 2
·Orthopedic
HYDROPHILIC GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
CENTERVUE MACULAR INTEGRITY ASSESSMENT
FDA 510(k)
FDA Class 2
·Ophthalmic
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·September 3, 2011
CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·July 18, 2013
HEARTSTART MRX -EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 18, 2015