562 results · 41ms · Sources: EU EUDAMED, US FDA

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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