19 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
9616240-2006-00344
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00342
FDA Adverse Event
Malfunction
·Product code KDI·June 14, 2006
9616240-2006-00330
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006
9616240-2006-00349
FDA Adverse Event
Malfunction
·Product code FII·June 21, 2006
9616240-2006-00348
FDA Adverse Event
Malfunction
·Product code FDI·June 20, 2006
*
FDA Adverse Event
Malfunction
·Product code FII·June 1, 2006
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 12, 2025
INSET I
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 12, 2025
9616240-2006-00346
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
SENSORMEDICS 3100A
FDA Adverse Event
Injury
·SENSORMEDICS·Product code LSZ·March 13, 2013
MICRO_TECH
FDA Adverse Event
Injury
·STANLEY SECURITY SOLUTIONS, INC. - SENIOR TECHNOLOGIES DIVISON·Product code KMI·February 24, 2011
RIATA ACTIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·May 1, 2014
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·April 28, 2014
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·March 27, 2014