Fentanyl is a synthetic opioid, up to 100 times more potent than morphine. Ingesting a small amount of fentanyl can be lethal. It is sometimes sold as, or mixed with heroin, pressed into tablets, and used as a cutting agent in other drugs.
Fentanyl is a synthetic opioid, up to 100 times more potent than morphine. Ingesting a small amount of fentanyl can be lethal. It is sometimes sold as, or mixed with heroin, pressed into tablets, and used as a cutting agent in other drugs.
This fentanyl test is a rapid, visual test for fentanyl. With it, you can determine if your sample contains fentanyl. The detection limit of this test is 200ng/ml. This is the best fentanyl test kit on the market and has an accuracy rate of 99.2%.
This fentanyl test kit includes 1 fentanyl test, which can be used on:
Powders
Liquids
Tablets
Surface Residue
Disclaimer
* A negative result can be interpreted as soon as both the test (T) and control (C) lines appear. A positive result can be interpreted once the control line has appeared and the background has cleared to white, typically by 60 seconds. Do not read results after 10 minutes.
The test device is NOT intended to determine the purity, composition, or if the substance being examined is safe to use.
A positive or negative test result is NOT an indication that the substance being examined is safe to use. Many factors come into play when examining the samples, including but not limited to mixture of multiple substances, solubility, and pH of the sample.
BTNX Inc. does not encourage the use, supply, or production of illegal drugs or controlled substances in any way. The device is intended for harm reduction purposes. Follow the advice of your local harm reduction or public health agency.
There is a possibility that technical or procedural errors as well as other substances and factors may interfere with the Rapid Response™ Fentanyl Test Strip (Liquid/Powder) and cause false results.
A positive result indicates the presence of fentanyl only and does not indicate quantity.
A negative result does not at any time rule out the presence of fentanyl, as they may be present below the minimum detection level of the test.
The following table lists compounds that are positively detected in oral fluid by The FYL Rapid Test Panel at 5 minutes.
Compound Concentration (ng/mL)
Alfentanyl >600,000
Fenfluramine 100000
Norfentanyl 40
Buspirone 3000
Fentanyl 200
Sufentanyl 100000
Package contents
1 Fentanyl Rapid Test
1 Bottle of Buffer
Instructions and product insert
Directions For Use
Test device (in closed pouches), samples, and controls should be brought to room temperature (15-30°C) prior to testing. Do not open pouches until ready to perform the assay.
Remove the test device from its protective pouch and label the device with patient’s identification or control label.
FOR SURFACES:
Remove the panel cap and wipe the panel over the surface in which the drugs are suspected.
With the arrow pointing toward the water, immerse the test panel vertically in the water for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.
Wait for the coloured lines to appear, read the results at 5 minutes. Do not interpret the results after 10 minutes.
Test device (in closed pouches), samples, and controls should be brought to room temperature (15-30°C) prior to testing. Do not open pouches until ready to perform the assay.
Remove the test device from its protective pouch and label the device with patient’s identification or control label.
FOR SURFACES:
Remove the panel cap and wipe the panel over the surface in which the drugs are suspected.
With the arrow pointing toward the water, immerse the test panel vertically in the water for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.
Wait for the coloured lines to appear, read the results at 5 minutes. Do not interpret the results after 10 minutes.
FOR SURFACES
FOR SOLIDS:
Prepare specimen collection containers and solid sample.
Pour solid sample into the specimen collection containers.
At least 1mg solid diluted with 5mL water (1 mineral water bottle cap equals roughly 5mL). Shake to mix well.
Remove the panel cap, with the arrow pointing toward the water, immerse the test panel vertically in the diluted specimen for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.
Wait for the coloured lines to appear, read the results at 5 minutes. Do not interpret the results after 10 minutes.
FOR SOLIDS
FOR URINE:
Collect urine in a clean and dry container.
Remove the panel cap, with the arrow pointing toward the specimen, immerse the test panel vertically in the specimen for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.
Wait for the coloured lines to appear, read the results at 5 minutes. Do not interpret the results after 10 minutes.
FOR URINE
INTERPRETATION OF RESULTS(Please refer to the illustrations above)
NEGATIVE:* A coloured line appears in the Control region (C) and coloured lines appear in the Test region (T). This negative result means that the concentrations in the sample are below the designated cut-off levels for a particular drug tested.
*NOTE: The shade of the coloured lines(s) in the Test region (T) may vary. The result should be considered negative whenever there is even a faint line.
POSITIVE: A coloured line appears in the Control region (C) and NO line appears in the Test region (T). The positive result means that the drug concentration in the sample is greater than the designated cut-off for a specific drug.
INVALID: No line appears in the Control region (C). Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for Control line failure.
Read the directions again and repeat the test with a new test card. If the result is still invalid, contact your manufacturer.
QUALITY CONTROL:
A procedural control is included in the test. A colored line appearing in the control line region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.
Control standards are not supplied with this kit; however, it is recommended that positive and negative controls be tested as good laboratory testing practice to confirm the test procedure and to verify proper test performance.
LIMITATIONS:
The FYL Surface Test Panel provides only a qualitative preliminary result. A secondary analytical method must be used to obtain a confirmed result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method.
A negative result may not necessarily indicate drug-free sample. Negative results can be obtained when drug is present but below the cut-off level of the test.
This test does not distinuish between drugs of abuse and certain medications.
EXPECTED VALUES:
The negative result indicates that the drug concentration is below the detectable level. Positive result means the concentration of drug is above the detectable level.
