BEUDAMED
    6 results · 24ms · 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 ×

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 7, 2014

    CAPTURE-R READY-SCREEN (3)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·October 3, 2012

    STARCLOSE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·July 21, 2010

    STANDARD INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·June 14, 2013

    HOLDING DEVICE FOR GUIDE WIRESAND REAMING RODS

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·June 14, 2013

    AIMING ARM FOR TI CANNULATED TIBIAL NAILS-EX

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·June 14, 2013