11 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
QUICK SET PARADIGM
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·June 3, 2024
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·December 25, 2024
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·January 2, 2025
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·December 13, 2024
MINIMED QUICK-SET
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·January 19, 2025
TOTAL ASR FEM IMP SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·March 14, 2013
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 1, 2011
CORDIS SV-5 X 300 CM
FDA Adverse Event
Injury
·CORDIS - ENDOVASCULAR·Product code DQX·February 26, 2008
HAND PIECE FOR BATTERY POWERED DRIVER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·August 5, 2015
HAND PIECE FOR BATTERY POWERED DRIVER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·August 5, 2015
HAND PIECE FOR BATTERY POWERED DRIVER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·August 5, 2015