BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    AMVISC (SODIUM HYALURONATE

    MDR report key: 32256 · Received April 25, 1996

    Report

    Report Number
    MW4001154
    Event Type
    Malfunction
    Date Received
    April 25, 1996
    Date of Event
    February 25, 1996
    Report Date
    March 29, 1996
    Manufacturer
    CHIRON VISION CORP.
    Product Code
    LZP
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    THE COMPLAINT WAS INVESTIGATED AND THE PRODUCT WAS EVALUATED AND NO MDR REPORT IS REQUIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AMVISC (SODIUM HYALURONATE VISCOELASTIC SURGICAL AID, 12 MG, 0.8 ML SYRINGE LZP CHIRON VISION CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA