10 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC.·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC.·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS, INC.·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC.·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC·Product code NCD·February 3, 2016
CELLESTIS
FDA Adverse Event
Malfunction
·CELLESTIS INC.·Product code NCD·February 3, 2016
UNK
FDA Adverse Event
Injury
·CELLESTIS INC·Product code NCD·July 10, 2013