BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 438944 · Received January 15, 2003

    Report

    Report Number
    2242056-2003-00001
    Event Type
    Injury
    Date Received
    January 15, 2003
    Date of Event
    December 26, 2002
    Report Date
    January 14, 2003
    Manufacturer
    ALTO DEVELOPMENT CORP./DBA A&E MEDICAL CORP.
    Product Code
    GEI
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * ELECTROSURGICAL ELECTRODE GEI ALTO DEVELOPMENT CORP./DBA A&E MEDICAL CORP. NA 009E

    Patients

    Seq Age Sex Outcome Treatment
    1