BEUDAMED
    FDA Adverse Event Other Summary report: N

    STERIS ALL-PURPOSE ARMBOARD

    MDR report key: 299032 · Received September 29, 2000

    Report

    Report Number
    1043572-2000-00005
    Event Type
    Other
    Date Received
    September 29, 2000
    Date of Event
    June 29, 2000
    Report Date
    July 5, 2000
    Manufacturer
    STERIS CORP.
    Product Code
    FWZ
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STERIS ALL-PURPOSE ARMBOARD * FWZ STERIS CORP. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *