BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ALLEGRETTO WAVE EYE-Q

    MDR report key: 2161062 · Received June 16, 2011

    Report

    Report Number
    3003288808-2011-00113
    Event Type
    Malfunction
    Date Received
    June 16, 2011
    Date of Event
    January 20, 2010
    Report Date
    January 20, 2010
    Manufacturer
    WAVELIGHT GMBH
    Product Code
    LZS
    PMA / PMN Number
    P030008/P02
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SZ
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    DURING THE ONSITE INVESTIGATION, THE SERVICE TECH INSTALLED AN UPGRADE TO THE BED CONTROLLER. ROOT CAUSE WAS DETERMINED TO BE DUE TO THE NEED FOR A BED CONTROLLER UPGRADE. (B)(4).

    Description of Event or Problem · 1

    PHYSICIAN REPORTS THE BED MOVES ON ITS OWN WITHOUT USER INTERVENTION. NO PT HARM WAS REPORTED AND NO FURTHER INFO HAS BEEN PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALLEGRETTO WAVE EYE-Q OPHTHALMIC EXCIMER LASER SYSTEM LZS WAVELIGHT GMBH 8065990631 NA

    Patients

    Seq Age Sex Outcome Treatment
    1