BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACUFEX MOSAIC PLASTY-TUBULAR CHISEL 3.5MM

    MDR report key: 82833 · Received April 4, 1997

    Report

    Report Number
    1219602-1997-00023
    Event Type
    Malfunction
    Date Received
    April 4, 1997
    Date of Event
    March 6, 1997
    Manufacturer
    SMITH & NEPHEW, INC. ENDOSCOPY DIV.
    Product Code
    KDG
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACUFEX MOSAIC PLASTY-TUBULAR CHISEL 3.5MM BONE CHISEL KDG SMITH & NEPHEW, INC. ENDOSCOPY DIV. NA 196

    Patients

    Seq Age Sex Outcome Treatment
    1 *