6 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Other
×
COULTER LH 750
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code GKZ·June 27, 2007
CD1800 ANALYZER
FDA Adverse Event
Other
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·June 29, 2007
CELL-DYN 1700
FDA Adverse Event
Other
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·December 2, 2004
LIPPES LOOP DOUBLE S INTRAUTERING DEVICE
FDA Adverse Event
Other
·R.W. JOHNSON PHARM RESEARCH INSTITUTE·Product code HDT·August 5, 1997
LIPPES LOOP DOUBLE S INTRAUTERINE DEVICE
FDA Adverse Event
Other
·R.W. JOHNSON PHARM. RESEARCH INSTITUTE·Product code HDT·August 5, 1997
ALL-FLEX ARCHING SPRING DIAPHRAGM
FDA Adverse Event
Other
·R.W. JOHNSON PHARM. RES. INST. USA/DIV. OF ORTHO PHARMACEUTICAL CORP.·Product code HDW·March 22, 2001