BEUDAMED
    FDA Adverse Event Summary report: N

    *

    MDR report key: 95446 · Received May 30, 1997

    Report

    Report Number
    2021283-1997-00024
    Date Received
    May 30, 1997
    Date of Event
    April 16, 1997
    Product Code
    FRN
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    MANUFACTURER'S REPORT DATE 3/10/1998.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * FRN 1340 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *