BEUDAMED
    4 results · 67ms · Sources: EU EUDAMED, US FDA

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    LASER FIBER

    FDA Adverse Event
    Injury ·ECLIPSE SURGICAL TECHNOLOGIES, INC.·Product code GEX·July 10, 1996

    MODEL 550-E1

    FDA Adverse Event
    Malfunction ·ECLIPSE SURGICAL TECHNOLOGIES, INC.·Product code LNK·April 18, 1997

    LASER PRIME

    FDA Adverse Event
    Death ·ECLIPSE SURGICAL TECHNOLOGIES, INC.·Product code LPC·February 16, 1993

    Advena Limited

    Authorized representative
    🇲🇹 Malta·467 Manufacturers·13717 Devices