Testsealabs BUP Buprenorphines Test
Intended Use
The One Step Buprenorphine Test Device is a lateral flow chromatographic immunoassay for the detection of Buprenorphine in human urine at a level relative to the Buprenorphine cut-off concentration of 10 ng/mL. This assay is intended for use by professionals to assist in the determination of drug compliance.
This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) or Liquid chromatography/mass spectrometry (LC/MS) are the preferred confirmatory methods. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.
Test Procedure:
Allow the test device, urine specimen, and/or controls to equilibrate to room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 100ml) to the specimen well (S) of the test device, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration above.
3. Wait for the red line(s) to appear. The result should be read at 5 minutes. It is important that the background is clear before the result is read. Do not interpret the result after 10 minutes.
How To Read Results:
Negative: *Two lines appear. One red line should be in the control region (C), and another apparent red or pink line adjacent should be in the test region (T). This negative result indicates that the drug concentration is below the detectable level.
*NOTE: The shade of red in the test line region (T) will vary, but it should be considered negative whenever there is even a faint pink line.
Positive: One red line appears in the control region (C). No line appears in the test region (T). This positive result indicates that the drug concentration is above the detectable level.
Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test using a new test panel. If the problem persists, discontinue using the lot immediately and contact your local distributor.
FAQs:
Q: What are your price?
A: Our price are subject to change depending on supply and other market factors. We will send you an updated price list after your company contact us for further information.
Q: Do you have a minimum order quantity?
A : Yes, require all international orders to have an ongoing minimum order quantity. If you are looking to resell but in much smaller quantities, we recommend you check our our website.
Q: Can you supply the relevant documentation?
A: Yes, we can provide most documentation including certificates and other export documents where required.
Q: Can you make OEM or ODM service?
A: Yes. We can accept OEM service. Meanwhile it's also welcome to choose our ODM products.
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