8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KINEMAX TIBIAL STEM EXTENSION
FDA 510(k)
FDA Class 2
·Orthopedic
SPECTRA ULTRASOUND SYSTEM W/COLOR FLOW MODULE
FDA 510(k)
FDA Class 2
·Radiology
EMIT(R) D.A.U. AMPHETAMINE CLASS MEDIUM CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Toxicology
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 26, 2024
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 26, 2024
SNOWDEN-PENCER LAPAROSCOPIC RAPTOR GRASPER
FDA Adverse Event
Malfunction
·CAREFUSION 2200 INC·Product code GCJ·June 3, 2014
VISCOJECT 1.8 DELIVERY SYSTEM
FDA Adverse Event
Injury
·MEDICEL AG·Product code MSS·December 28, 2012
IDENTITY ADX DR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010