BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2925153-2001-00009

    MDR report key: 346542 · Received June 30, 2001

    Report

    Report Number
    2925153-2001-00009
    Event Type
    Injury
    Date Received
    June 30, 2001
    Date of Event
    March 26, 2001
    Product Code
    HOC
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    30446 HOC

    Patients

    Seq Age Sex Outcome Treatment
    1