BEUDAMED
    FDA Adverse Event Other Summary report: N

    CMI

    MDR report key: 266538 · Received March 3, 2000

    Report

    Report Number
    266538
    Event Type
    Other
    Date Received
    March 3, 2000
    Date of Event
    February 24, 2000
    Report Date
    February 24, 2000
    Manufacturer
    CMI
    Product Code
    HDB
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    TIME OF DELIVERY, 19:00 ON 02/24/2000. BRUISING, EDEMA AND NICKEL SIZE ABRASION NOTED ON OCCIPITAL AREA OF BABY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CMI MANUAL VACUUM EXTRACTOR HDB CMI * *

    Patients

    Seq Age Sex Outcome Treatment
    1 0 DAY Other