BEUDAMED
    5 results · 28ms · 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 ×

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·February 21, 2013

    TRIMA AUTOMATED BLOOD COLLECTION SYSTEM

    FDA Adverse Event
    CARIDIAN·Product code LKN·January 14, 2011

    GENESYS HTA PROCERVA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code MNB·August 1, 2014

    HANDLE WITH QUICK COUPLING- SMALL

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code OVE·September 6, 2016

    AIM-ARM RADIOLUC F/GREATER TROCHANTER FE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HSB·October 24, 2022