7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
INTERMOORE FRACTURE HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
SYSTEMS OF SIGHT LOW VISION EYEWARE
FDA 510(k)
FDA Class 1
·Ophthalmic
RUBEOLA IGG ELISA TEST
FDA 510(k)
FDA Class 1
·Microbiology
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·November 17, 2017
CAPSUREFIX MRI
FDA Adverse Event
Injury
·MPRI·Product code NVN·February 11, 2013
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·July 24, 2014