BEUDAMED
    6 results · 36ms · 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 ×

    IMPELLA CP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·December 26, 2025

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·February 8, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 22, 2014

    LOGIC TIBIA PS MOD INSRT SZ 5 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 19, 2023

    LOGIC FEMORAL PS CEM RIGHT SZ 5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 2, 2024