BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA × Status: Injury × Clear all

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·January 13, 2017

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·January 13, 2017

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 5, 2014

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 4, 2010

    INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 20, 2012

    UNK - PLATES: 2.0 MM LOCK MANDIBLE MINIPLATE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·September 16, 2021

    UNK - PLATES: 2.0 MM LOCK MANDIBLE MINIPLATE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·September 16, 2021

    UNK - SCREWS: LOCKING: MANDIBLE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·September 16, 2021

    HEARTWARE VENTRICULAR ASSIST SYSTEM- PUMP

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·March 22, 2018