cobas® liat CT/NG

IVD For in vitro diagnostic use.
cobas liat CT/NG assay

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Trusted sexual health testing for everybody, in every setting

1 in 5 people have an STI—totaling more than 68 million.1  Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) are among the most common, treatable STIs. Although chlamydia and gonorrhea may present with similar symptoms, each requires a different treatment approach, making accurate diagnosis essential. Syndromic management, which often leads to over- or under-treatment, is considered a major driver of antimicrobial resistance (AMR).

The cobas® liat CT/NG assay delivers fast, accurate results for all genders, providing confidence in sexual health status. With results in just 20 minutes, you can test and treat during the patient visit, ensuring timely and appropriate care. 

cobas® liat CT/NG specifications

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cobas® liat CT/NG specifications

Instrument

cobas® liat system

Targets

Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG)

Registration

FDA 510(k) cleared, CLIA-waived

Time to result

20 minutes

Sample type

Male urine, vaginal swabs (clinician collected and self-collected in a clinical setting)

Reagents

Ready-to-use, pre-packed tube format

Kit Storage

2–8°C

Collection media

cobas® PCR Media

Technology

Real-time PCR

Sample extraction

Fully automated and integrated

Control

Internal sample processing control, positive and negative controls

cobas® liat CT/NG ordering information

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cobas® liat CT/NG ordering information

Material Number

Alternative Catalog Number

Material Description

Pack Size

Pack size Description

10030933190   KIT COBAS LIAT CT/NG 1 pack 20 tests
09449639190   KIT COBAS LIAT CT/NG/MG QC 1 pack 3 sets
07958030190   cobas PCR Media Uni Swab Sample Kit 1 pack 100 uni swab sample packets
05170486190   COBAS PCR MEDIA URINE SAMPLE KIT 1 pack 100 Urine Sample Packets
<b>cobas</b><sup>®</sup> <b>liat</b> CT/NG intended use<sup>2</sup>

cobas® liat CT/NG intended use2

The cobas® liat CT/NG nucleic acid test is an automated, qualitative in vitro nucleic acid diagnostic test that utilizes real-time polymerase chain reaction (PCR) for the direct detection of Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) nucleic acid in male urine and vaginal swabs in cobas® PCR Media (Roche Molecular Systems, Inc.).

This test is intended as an aid in the diagnosis of urogenital infections in both symptomatic and asymptomatic individuals.

Would you like to know more about the cobas® liat CT/NG assay?

Please submit your information in the following form to be contacted by a Roche representative with more details about the cobas® liat CT/NG assay.

References

  1. World Health Organization, Sexually Transmitted Infections https://www.who.int/health-topics/sexually-transmitted-infections#tab=tab_1. Accessed 1/14/2025.
  2. cobas® liat CT/NG IVD Instructions for Use

Overview

Detailed Specifications

Ordering Information

Compatible Instruments

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    Technical Documents

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