FreeStyle Libre 14 day Sensor Kit


Product Overview

FreeStyle Libre 14 day Sensor Kit
FreeStyle Libre 14 day - 71940


Device Description

An assembly of electrically-powered, portable devices intended to continuously monitor interstitial-fluid glucose concentrations in a patient with diabetes mellitus, using an invasive electrochemical technique. It consists of an electrochemical, percutaneously-inserted electrode that physically connects to a cable or transmitter which communicates with a monitor or receiver (not included) that captures, stores, and converts the sensor signals to glucose concentrations for display. The system may be used in the home and clinical settings, and aids in the detection of episodes of hyperglycaemia and hypoglycaemia, facilitating acute/long-term therapy adjustments.


Environmental Conditions

  • Storage Environment Atmospheric Pressure - KiloPascal
    • 106000.00
    • 70000.00
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 90.00
    • 10.00
  • Storage Environment Temperature - Degrees Fahrenheit
    • 77.00
    • 39.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: PZE

    Device Name: Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-Initiated

    Device Class: 3

    Physical State: This device comprises a skin piercing sensor containing the glucose specific biological sensor, an algorithm that converts sensor signals into glucose values, a display device which provides glucose values to the user and a mechanism for transmitting data from the sensor to the display device.

    Definition: A subcutaneous factory calibrated, non-adjunctive, invasive, passive monitoring glucose sensor is intended to determine glucose levels and the direction and rate of change of glucose levels in people with diabetes. Calibrated at the point of manufacture and does not require or accept any user-entered calibration. Monitors glucose levels passively and only provides information, including alarms and alerts, in response to a user initiated action. The device is indicated to replace information obtained from standard blood glucose monitoring devices to make diabetes-related treatment decisions and also provides historical glucose information, facilitating long-term therapy adjustments.

    Submission Type ID: 2

    Review Panel: CH

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Signals from an invasive (skin piercing) glucose specific biological sensor are algorithmically converted to glucose values which are provided to the user.

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: Interstitial fluid.

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Device Identifiers

    Device Id: 30357599001019

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 00357599001018

    Package Quantity: 24

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: Case


    Device Id: 00357599001018

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


    Device Id: 57599-0001-01

    Device Type: Secondary

    DeviceId Issuing Agency: NDC/NHRIC

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


    Educational Resources
    Videos