9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
UNKNOWN COOLSCULPTING® SYSTEM
FDA Adverse Event
Injury
·ALLERGAN PLEASANTON·Product code OOK·December 5, 2021