BEUDAMED
    4 results · 21ms · 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 ×

    ALTRX NEUT 36IDX56OD

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code LPH·April 3, 2013

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 25, 2011

    SIMVIEW 3000

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS·Product code KPQ·April 15, 2008

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 21, 2017