8 results
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38ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FLOEY CATHETER W TEMP
FDA Adverse Event
Injury
·DEGANIA SILICONE LTD·Product code DRF·October 17, 2017
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·DEGANIA SILICONE LTD.·Product code KOD·July 7, 2017
AU480 CLINICAL CHEMISTRY ANALYZER WITH ISE
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JGS·May 25, 2014
FORCEPS MCL19 LEFT BOUCHAYER HEART [MXI/XOM]
FDA Adverse Event
XOMED MICROFRANCE MFG·Product code LRC·November 14, 2012
EPIC II VR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2010
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·MMJ SA DE CV (USD)·Product code DRF·November 9, 2018