BEUDAMED
    10 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 ×

    MEDIAL ROTATION KNEE

    FDA Adverse Event
    Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

    MEDIAL ROATION KNEE

    FDA Adverse Event
    Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

    MEDIAL ROATION KNEE

    FDA Adverse Event
    Injury ·MATORHTO LIMITED·Product code JWH·January 22, 2016

    MEDIAL ROTATION KNEE

    FDA Adverse Event
    Malfunction ·MATORTHO LIMITED·Product code JWH·January 22, 2016

    MEDIAL ROTATION KNEE

    FDA Adverse Event
    Injury ·MATORTHO LIMITED·Product code JWH·January 22, 2016

    BD¿ GRAVITY IV SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·December 9, 2021

    RECON LOCKING AIMING ARM FOR LATERAL ENTRY FEMORAL NAILS-EX

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code FZX·March 25, 2013

    OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·TRIVASCULAR, INC.·Product code MIH·August 19, 2014

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSH·March 25, 2008

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·August 3, 2020