10 results
·
34ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
HEMOCCULT® ICT TEST DEVICE
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code KHE·June 3, 2013
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, PUERTO RICO, B.V.·Product code MGB·October 16, 2008
OT ULTRA TEST STRIPS
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 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