BEUDAMED
    FDA Adverse Event Other Summary report: N

    VAGINAL SPECULUM

    MDR report key: 19058780 · Received April 5, 2024

    Report

    Report Number
    MW5153593
    Event Type
    Other
    Date Received
    April 5, 2024
    Report Date
    April 4, 2024
    Manufacturer
    TRINITY STERILE, INC.
    Product Code
    HDF
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    LIGHTS BREAKING OFF OF SPECULUM WHEN OPENING PACKAGE. REFERENCE REPORT: MW5153592.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    540852 VAGINAL SPECULUM SPECULUM, VAGINAL, METAL HDF TRINITY STERILE, INC. 22201 56277

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown