BEUDAMED
    41 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·May 12, 2009

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·September 11, 2009

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·August 30, 2010

    MAESTRO MEDIUM FIXED DURAGUARD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBB·May 20, 2014

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·CARROLL HEALTHCARE·Product code FNL·November 5, 2012

    FLEXIMA CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FFA·August 30, 2010

    HYALURONIC ACID (BRAND NAME NOT REPORTED)

    FDA Adverse Event
    Other ·UNK·Product code LMH·May 27, 2010

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·May 1, 2009

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·May 14, 2009

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·June 10, 2009

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·May 6, 2009

    RESTYLANE INEJCTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·September 10, 2009

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    ADAPTA D

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·July 24, 2009

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2015

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·March 27, 2015

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·May 1, 2018