BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDI-JECTOR

    MDR report key: 269971 · Received March 17, 2000

    Report

    Report Number
    2182861-2000-00001
    Event Type
    Other
    Date Received
    March 17, 2000
    Report Date
    March 3, 2000
    Manufacturer
    MEDI-JECT CORP
    Product Code
    KZE
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PT EXPERIENCED A BLOOD SUGAR READING OF 28 AND WAS TAKEN TO THE EMERGENCY ROOM WHERE GLUCOSE TABLETS WERE GIVEN TO RETURN THE BLOOD SUGAR TO A SAFE LEVEL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDI-JECTOR NEEDLE-FREE INSULIN INJECTION SYSTEM KZE MEDI-JECT CORP 300123-002 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other