6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COORDINATE REVISION KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ARTHROSCOPIC RETRACTORS AND GRASPERS
FDA 510(k)
FDA Class 2
·Orthopedic
VIDAS CHLAMYDIA ASSAY, MODIFICATION
FDA 510(k)
FDA Class 1
·Microbiology
PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES
FDA Adverse Event
MEDEL S.P.A.·Product code BTI·February 11, 2013
TENDRIL DX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011
ENDURANT II
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·July 24, 2014