10 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
LIGHTSTRIKE ROBOT
FDA Adverse Event
Malfunction
·XENEX DISINFECTION SERVICES INC.·Product code MKB·December 20, 2022
OCCLUSION BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORK LTD.·Product code KOD·October 3, 2007
OCCLUSION BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORK LTD.·Product code KOD·October 3, 2007
INFLOW TUBING FMS VUE 24PK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·June 28, 2021
INFLOW TUBING FMS VUE 24PK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·June 28, 2021
RUSCH AGT NASAL PERFORMED ET TUBE, 7.0MM
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BSK·March 8, 2013
LIGASURE ATLAS HANDSWITCHING 37CM
FDA Adverse Event
Malfunction
·COVIDIEN LLP (SHANGHAI)·Product code GEI·February 18, 2011
INFLOW TUBING FMS VUE 24PK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·June 29, 2021
INFLOW TUBING FMS VUE 24PK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·June 29, 2021
INFLOW TUBING FMS VUE 24PK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HRX·June 29, 2021