BEUDAMED
    FDA Adverse Event Other Summary report: N

    HP

    MDR report key: 303539 · Received November 8, 2000

    Report

    Report Number
    303539
    Event Type
    Other
    Date Received
    November 8, 2000
    Date of Event
    October 31, 2000
    Report Date
    November 8, 2000
    Manufacturer
    AGILENT TECHNOLOGIES
    Product Code
    LDD
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT DEFIBRILLATED WITHOUT GEL, BURNED SKIN. THIS WAS AN EMERGENT SITUATION. NO TIME TO USE GEL PAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HP DEFIBRILLATION LDD AGILENT TECHNOLOGIES M1722A *

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Other