8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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S-ROM/NOILES MARK 3
FDA 510(k)
FDA Class 2
·Orthopedic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756656429·HEAD AND NECK PACK
Arm Extension Cross Bar
FDA UDI
KOROS U.S.A., INC.·10840199538697·Arm Extension Cross Bar
MALIS BIPOLAR CORD/IRRIGATION TUBING SET
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
QUIK-DOT TOXOPLASMOSIS
FDA 510(k)
FDA Class 2
·Microbiology
THUNDERBEAT 5 MM, 35 CM, FRONT ACTUATED GRIP
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code GEI·May 20, 2014
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 10, 2010
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·November 20, 2012