The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS or LC/MS is the preferred confirmatory method.
This kit is only used to monitor the fentanyl content in the urine of drug addicts. It is a non-medical device cannot treat drug addiction. It does not have clinical diagnostic significance.
This kit uses highly specific antibody drug coupling agent reaction and immunochromatographic analysis technology. The reagent contains drug conjugate coupling agent pre fixed on the membrane test region (T) and antibody conjugate on the binding pad.
During testing, drop the urine sample directly into the sampling hole of the detection card. If it is negative, the urine does not bind to the antibody conjugate on the binding pad, and the antibody conjugate on the binding pad binds to drug conjugate coupling agent, resulting in a red band in the test region. If it is positive, the drugs in the urine will react with the antibody conjugate first. When the drug content in the urine reaches a certain amount, the antibody conjugate on the binding pad will no longer bind to the specific drug coupling agent in the test region, and there will be no colored line in the test region (T).
Regardless of whether drugs are present in urine or not, a colored line will appear in the quality control region (C). The colored line displayed in the quality control region (C) is a standard for determining whether there is sufficient urine sample and whether the chromatography process is normal, and also serves as an internal control standard for the reagent.
| Product Name | Fentanyl (FENT) Rapid Test (Immunochromatographic Assay) |
| Model | ICA2506-14 |
| Sample | Urine |
| Storage Condition | 2~30℃（35.6~86℉） |
| Cut-off | 1 ng/ml |
| Shelf Life | 24 months |
| Classification | GPSR(EU) |
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