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Description
cobas™ liat CT/NG/MG control kit for use with the cobas™ liat CT/NG/MG assay or cobas™ liat CT/NG assay.
Specifications
Specifications
| Certifications/Compliance | CE |
| Content And Storage | 2°C to 8°C |
| Concentration | Positive: 3 x 0.3 mL; Negative: 3 x 0.3 mL |
| Detectable Analytes | Chlamydia trachomatis (CT) nucleic acids, Neisseria gonorrhoeae (NG) nucleic acids |
| Format | 3 sets of positive and negative controls per kit |
| For Use With (Equipment) | cobas™ liat analyzer CT/NG and CT/NG/MG assay kits |
| Sample Type | Urine, Swab |
| Type | IVD Control |
| Includes | 3 sets of positive and negative controls per kit |
| Intended Use | Control tests to be used for the cobas™ liat CT/NG and CT/NG/MG assays. The cobas™ liat CT/NG/MG test is an automated, qualitative in vitro nucleic acid diagnostic using real-time PCR for the detection of CT, NG, and MG in male urine and vaginal swabs. The cobas™ liat CT/NG test is an automated, qualitative in vitro nucleic acid diagnostic using real-time PCR for the detection of CT and NG in male urine and vaginal swabs. |
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