BEUDAMED
    22 results · 39ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PULSAR II REFURB GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·August 14, 2015

    GENERATOR PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·August 13, 2015

    GENERATOR PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code MUL·October 9, 2014

    GENERATOR PULSAR II REFURB

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·September 10, 2015

    PULSAR II GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCE ENERGY, LLC·Product code GEI·February 10, 2015

    PULSAR 2 GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code GEI·February 23, 2015

    PULSAR II GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code GEI·April 1, 2015

    GENERATOR PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code MUL·October 16, 2014

    GENERATOR PS100-102 PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code MUL·December 15, 2014

    PULSAR 2 GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code MUL·November 13, 2014

    STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·June 12, 2020

    PULSAR II GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code MUL·November 24, 2014

    GENERATOR PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code MUL·December 12, 2014

    GENERATOR PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY (SALIENT)·Product code GEI·April 1, 2016

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·June 27, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·January 7, 2013

    MAVERICK2 BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·November 16, 2010

    GENERATOR PULSAR II

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·February 10, 2015

    SMR CEMENTLESS REVISION STEM Ø13 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code PHX·July 1, 2024

    UNK JUVEDERM VOLUX

    FDA Adverse Event
    Injury ·ALLERGAN (PRINGY)·Product code LMH·March 8, 2024