The GLUCOCARD Shine Connex Blood Glucose Monitoring System is intended for the quantitative measurement of glucose in fresh capillary whole blood samples drawn from the fingertips and alternative sites such as the forearm, palm, thigh and calf.


Product Overview

The GLUCOCARD Shine Connex Blood Glucose Monitoring System is intended for the quantitative measurement of glucose in fresh capillary whole blood samples drawn from the fingertips and alternative sites such as the forearm, palm, thigh and calf.
GLUCOCARD® Shine Connex Blood Glucose Monitoring System - 543110


Device Description

A collection of devices including a portable, battery-powered, semi-automated or automated instrument (self-testing meter), reagents, test strips and/or other associated materials and accessories (e.g., control solutions, lancets) intended to be used for the quantitative measurement of glucose in a whole blood clinical specimen; it is designed to be used for self-testing by a layperson in the home, and some types may in addition be used at the point-of-care. Measured glucose values are used to manage blood glucose levels, primarily by persons with diabetes mellitus.


Environmental Conditions

  • Handling Environment Humidity - Percent (%) Relative Humidity
    • 90.00
    • 10.00
  • Handling Environment Temperature - Degrees Fahrenheit
    • 111.20
    • 42.80
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 80.00
    • 20.00
  • Storage Environment Temperature - Degrees Fahrenheit
    • 122.00
    • 32.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: NBW

    Device Name: System, Test, Blood Glucose, Over The Counter

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: CH

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 862.1345

    Third Party Flag: N

    Medical Specialty: CH


    Device Identifiers

    Device Id: 20015482543109

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 10015482543102

    Package Quantity: 16

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: Master Shipper


    Device Id: 10015482543102

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 00015482543105

    Package Quantity: 4

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: Case Shipper


    Device Id: 00015482543105

    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


    GMDN ®. © GMDN Agency 2005-2024.
    Educational Resources
    Videos