BEUDAMED
    5 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 ×

    TI PANGEA LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·June 5, 2012

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 29, 2013

    INTERSTIM

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·April 11, 2011

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 22, 2008

    TI PANGEA LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code NKB·June 5, 2012