BEUDAMED
    7 results · 58ms · 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.

    NI

    FDA Adverse Event
    Malfunction ·MEDI-SOURCE, INC.·Product code KEW·August 6, 1998

    RYAN 102C REUSABLE ELECTRODES

    FDA Adverse Event
    Injury ·MEDI-SOURCE, INC.·Product code GXY·December 2, 2005

    NI

    FDA Adverse Event
    Malfunction ·MEDI-SOURCE INC.·Product code KEW·May 13, 1998

    ECO-MED ULTRA SOUND GEL

    FDA Adverse Event
    Injury ·Product code ITX·September 9, 2021

    Obelis s.a.

    Authorized representative
    🇧🇪 Belgium·546 Manufacturers·18515 Devices

    Sungo Cert GmbH

    Authorized representative
    🇩🇪 Germany·173 Manufacturers·3269 Devices

    Advena Limited

    Authorized representative
    🇲🇹 Malta·467 Manufacturers·13717 Devices