BEUDAMED
    6 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 ×

    MARA PROBE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MNB·May 12, 2022

    GS

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code MKJ·June 28, 2022

    NOVUM IQ

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 13, 2025

    ZENITH AAA ENDOVASCULAR GRAFT AAA ANCILLARY COMPONENT MAIN BODY EXTENSION

    FDA Adverse Event
    Injury ·COOK, INC.·Product code MIH·October 23, 2008

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·August 8, 2011

    LCS COMP RP INSERT LG+ 10MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC·Product code NJL·July 8, 2013