6 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BONE ANCHOR SYSTEM III (BAS III)
FDA 510(k)
FDA Class 2
·Orthopedic
Confirm Rx Insertable Cardiac Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
BODYVIZ, MODEL 100
FDA 510(k)
FDA Class 2
·Radiology
CONSERVE(R) TOTAL HEAD W/BFH
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 5, 2013
ENRHYTHM DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·February 15, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 7, 2014