The Aptima® System Fluid Preservative Kit is used with the Aptima® Assays on the Tigris® DTS® System. Use the System Fluid Preservative Kit according to the instructions outlined in the appropriate assay package insert and the Tigris® DTS® System Operator’s Manual.


Product Overview

The Aptima® System Fluid Preservative Kit is used with the Aptima® Assays on the Tigris® DTS® System. Use the System Fluid Preservative Kit according to the instructions outlined in the appropriate assay package insert and the Tigris® DTS® System Operator’s Manual.
Aptima® - KIT, AC2 SYS FL PRES,TIG,IVD-CE (302380)


Device Description

A collection of reagents and other associated materials intended to be used to optimise an assay performed using a nucleic acid technique (NAT) on a clinical specimen. The kit typically consists of a silicone oil to minimize evaporation, buffered solutions for washing steps and reaction stop reagents.


Environmental Conditions

  • Storage Environment Temperature - Degrees Celsius
    • 30.00
    • 15.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: LSL

    Device Name: Dna-Reagents, Neisseria

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: MI

    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: 866.3390

    Third Party Flag: N

    Medical Specialty: MI


    Code: MKZ

    Device Name: Dna Probe, Nucleic Acid Amplification, Chlamydia

    Device Class: 1

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: MI

    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: 866.3120

    Third Party Flag: Y

    Medical Specialty: MI


    Device Identifiers

    Device Id: 15420045500266

    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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