BEUDAMED
    FDA Adverse Event Other Summary report: N

    MILTEX

    MDR report key: 122689 · Received September 26, 1997

    Report

    Report Number
    2431021-1997-00010
    Event Type
    Other
    Date Received
    September 26, 1997
    Date of Event
    September 25, 1997
    Report Date
    September 26, 1997
    Manufacturer
    MILTEX INSTRUMENT CO.
    Product Code
    EJI
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    DR WAS ADMINISTERING MEDICATION WHEN FINGER RING BROKE IN HALF CAUSING INJURY TO THE DR. VERY SLIGHT CUT OCCURRED AT THUMB CREASE. BANDAGE WAS APPLIED, NO FURTHER ACTION WAS REQUIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MILTEX ASPIRATING SYRINGE EJI MILTEX INSTRUMENT CO. 76-70 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other