BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 229210 · Received June 23, 1999

    Report

    Report Number
    1832656-1999-00002
    Event Type
    Malfunction
    Date Received
    June 23, 1999
    Date of Event
    April 30, 1999
    Manufacturer
    BIOPRO, INC.
    Product Code
    HSH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * Implant * HSH BIOPRO, INC. NA 93-0845

    Patients

    Seq Age Sex Outcome Treatment
    1