7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RNS STERILE, DISPOSABLE AMNIOCENTESIS TRAY
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
CD 3700 SL
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007
133 SERIES BTE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
EXCEL DUOPAULSE MODEL 2000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ASR ACETABULAR IMPLANT 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 11, 2013
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·DEPUY INTL., LTD.8010379·Product code JDI·July 24, 2014
QUICKFLEX XL LV LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 10, 2011