BEUDAMED
    4 results · 29ms · 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 ×

    UNKNOWN SALINE IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·October 9, 2018

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLYNELLCOR PURITAN BENNETT IRELAND·Product code CBK·March 26, 2014

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 31, 2012

    CARTO¿ 3 SYSTEM

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, LTD (HAIFA, ISRAEL)·Product code DQK·August 24, 2010