The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma.


Product Overview

The device is intended for the quantitative in vitro determination of CK
CK-MB - CK4043


Device Description

A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of creatine kinase myocardial isoenzyme (CKMB) in a clinical specimen.


Environmental Conditions

  • Special Storage Condition, Specify
    • Once opened, the reagent is stable on board the analyzer for 28 days at +10°C.
  • Storage Environment Temperature - Degrees Celsius
    • 8.00
    • 2.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: CGS

    Device Name: Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

    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: 862.1215

    Third Party Flag: Y

    Medical Specialty: CH


    Device Identifiers

    Device Id: 05055273213973

    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


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