BEUDAMED
    4 results · 46ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·February 9, 2024

    PULSE GEN MODEL 106

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·January 19, 2024

    MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 25, 2022

    PUMP MMT-1781KL 670G MG RPL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 1, 2022