BEUDAMED
    8 results · 25ms · 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 ×

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DRA·October 27, 2008

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DRA·October 27, 2008

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 13, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·February 27, 2011

    2-DAY INFUSION KIT

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS KALAMAZOO·Product code MEB·February 18, 2008

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DRA·October 27, 2008

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DRA·October 27, 2008

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DYB·April 17, 2008