562 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Other
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MEDTRONIC SPINAL CORD STIMULATOR (NOT IN PROTOCOL)
FDA Adverse Event
Other
·Product code LGW·September 16, 2009
ABBOTT AXSYM SYSTEM
FDA Adverse Event
Other
·ABBOTT MFG., INC.·Product code JJE·October 6, 1997
ABBOTT AXSYM SYSTEM
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JJE·August 14, 1997
AXSYM CK-MB REAGENT
FDA Adverse Event
Other
·ABBOTT HEALTH PRODUCTS, INC.·Product code JHS·April 18, 1997
DASH 4000
FDA Adverse Event
Other
·GE HEALTHCARE·Product code MHX·February 24, 2009
AXSYM CK-MB REAGENT
FDA Adverse Event
Other
·ABBOTT HEALTH PRODUCTS, INC.·Product code JHS·July 17, 1997
SYNCHRON LX I 725 CLINICAL SYSTEM
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code JJE·June 20, 2006
1310P MEDITRACE 2/PK 20/CA
FDA Adverse Event
Other
·COVIDIEN·Product code MLN·May 11, 2012
1310P MEDITRACE 2/PK 20/CA
FDA Adverse Event
Other
·COVIDIEN·Product code DRX·March 25, 2013
1310P MEDITRACE 2/PK 20/CA
FDA Adverse Event
Other
·COVIDIEN·Product code MLN·January 18, 2013
1310 EDITRCE 2/PK 20/CA
FDA Adverse Event
Other
·TYCO HEALTHCARE·Product code LDD·May 12, 2005
1310P MEDITRACE 2/PK 20/CA
FDA Adverse Event
Other
·TYCO HEALTHCARE·Product code LDD·May 12, 2005
LACTOSORB 2.0X5MM SUSPENSION PUSH SCREW, 2PK
FDA Adverse Event
Other
·BIOMET MICROFIXATION·Product code MAI·August 19, 2008
LACTOSORB 2.0X5MM SUSPENSION PUSH SCREW, 2PK
FDA Adverse Event
Other
·BIOMET MICROFIXATION·Product code MAI·August 19, 2008
1210H MEDITRACE 2/PK 20/CA
FDA Adverse Event
Other
·COVIDIEN·Product code MLN·September 19, 2013
DELFLEX 2.5% DEX. LM 5L, 2-PK
FDA Adverse Event
Other
·OGDEN MANUFACTURING·Product code KPO·April 25, 2003
UNI-VENT
FDA Adverse Event
Other
·IMPACT INSTRUMENTATION, INC.·Product code CBK·January 28, 2012
SMART CAPNOLINE H PEDIATRIC
FDA Adverse Event
Other
·ORIDION MEDICAL 1987 LTD.·Product code CCK·March 22, 2012
EASYCAP II
FDA Adverse Event
Other
·COVIDIEN, FORMERLY TYCO·Product code CCK·March 2, 2012
VENTILATOR, CONTINUOUS, FACILITY USE.
FDA Adverse Event
Other
·RESPIRONICS INC·Product code CBK·February 14, 2012