2,160 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Other
×
NOVOPEN 3
FDA Adverse Event
Other
·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMF·October 16, 2012
PERLANE-L INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·December 30, 2011
RESTYLANE-L INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·April 1, 2011
SCULPTRA
FDA Adverse Event
Other
·GLOBAL PHARMACOVIGILANCE AND EPIDEMIOLOGY / SANOFI-AVENTIS·Product code LMH·June 7, 2007
SYNCHRON LX20
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code JJC·March 19, 2004
SYNCHRON LX20PRO
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code JGS·February 15, 2006
SYNCHRON LX I 725 CLINICAL SYSTEM
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code JJE·December 22, 2005
RAPIDLAB 1265
FDA Adverse Event
Other
·SIEMENS MEDICAL SOLUTIONS DIAGNOSTICS, LTD.·Product code KHP·March 1, 2010
AXSYM TOTAL BHCG
FDA Adverse Event
Other
·ABBOTT HEALTH PRODUCTS, INC.·Product code JHI·January 20, 2004
RAPIDLAB 1265
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING LTD.·Product code GKR·July 26, 2010
UNICEL DXC 800 PRO SYNCHRON CLINICAL SYSTEMS
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code JJE·June 19, 2007
NOVOFINE (30G)
FDA Adverse Event
Other
·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMI·July 2, 2007
IMX ANALYZER
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JHI·August 4, 2003
ARCHITECT I2000 ANALYZER
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JJE·January 20, 2006
PERLANE-L INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·September 1, 2011
SYSMEX XT-2000I
FDA Adverse Event
Other
·SYSMEX CORPORATION·Product code GKZ·February 5, 2008
SYSMEX XT-2000I
FDA Adverse Event
Other
·SYSMEX CORP·Product code GKZ·February 5, 2008
OPUS / AUTO CUFF
FDA Adverse Event
Other
·ARTHROCARE·Product code MBI·September 2, 2005
AEROSET ANALYZER
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JJE·September 14, 2000
ABBOTT AXSYM SYSTEM
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JJE·April 15, 2005