BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    WELCH ALLYN OPHTHALMOSCOPE BATTERY

    MDR report key: 9992335 · Received April 22, 2020

    Report

    Report Number
    MW5094241
    Event Type
    Malfunction
    Date Received
    April 22, 2020
    Report Date
    April 20, 2020
    Manufacturer
    UNK
    Product Code
    HLJ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    BATTERY BURNT ONCE PUT IN OPHTHALMOSCOPE. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    452440 WELCH ALLYN OPHTHALMOSCOPE BATTERY OPHTHALMOSCOPE, BATTERY-POWERED HLJ UNK 20-045

    Patients

    Seq Age Sex Outcome Treatment
    1