BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 141725 · Received December 31, 1997

    Report

    Report Number
    2647580-1997-01733
    Event Type
    Malfunction
    Date Received
    December 31, 1997
    Date of Event
    October 24, 1997
    Manufacturer
    *
    Product Code
    GAG
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    2/10/1998-SUPPLEMENTAL REPORT #1 SUBMITTED TO FDA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * GAG * * *

    Patients

    Seq Age Sex Outcome Treatment
    1