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Hangzhou AllTest Biotech CO.,LTD 

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My oldest daughter actually has Lyme disease. She spent almost 1 year in a wheelchair because of Lyme. She is doing very well now. I used 2 of the samples. 1 to test my Lyme diagnosed daughter and 1 to test my daughter who does not have Lyme. Your tests worked well. My daughter with Lyme tested positive and the one who does not tested negative.

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CE Certified Carfentanyl Rapid Test Panel , rapid diagnostic test kits

Product Details:

Place of Origin:CHINA
Brand Name:AllTest
Certification:CE, FDA 510K
Model Number:panel

Payment & Shipping Terms:

Minimum Order Quantity:500
Packaging Details:40T/kit
Supply Ability:100 Million a year
Detailed Product Description
Format: Panel Specimen: Urine
Kit Size: 40T/kit Cut-Off: 500 Ng/mL
Color: White Storage: 2-30°C

A rapid test for the qualitative detection of carfentanyl in human urine. For medical and other professional in vitro diagnostic use only CE certified

 

 

Applications: 

 

The Carfentanyl Rapid Test Panel (Urine) is a rapid immunochromatographic assay for the qualitative detection of carfentanyl. This test will detect other compounds, please refer to Analytical Specificity table in this package insert.

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) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

 

 

Description: 

 

Carfentanyl is an analog of the synthetic opioid analgesic fentanyl. It is 10,000 times more potent than morphine, making it among the most potent commercially used opioids. Carfentanil was first synthesized in 1974. 1 It is marketed under the trade name Wildnil as a general anaesthetic agent for large animals. 2 Side effects of carfentanil are similar to those of fentanyl, which include itching, nausea and respiratory depression, which can be life-threatening3. Carfentanil is classified as Schedule II under the Controlled Substances Act in the United States with a DEA ACSCN of 9743. 4

The Carfentanyl Rapid Test Panel (Urine) is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes a monoclonal antibody to selectively detect elevated levels of Carfentanyl in urine. The Carfentanyl Rapid Test Panel (Urine) yields a positive result when Carfentanyl in urine exceeds 500 ng/ml.

 

 

How to use? 

 

 

  • Allow the test, urine specimen, and/or controls to reach room temperature (15-30ºC) prior to testing.

    1. Bring the pouch to room temperature before opening it. Remove the test panel from the sealed pouch and use it within one hour.
    2. Remove the cap.
    3. With the arrow pointing toward the urine specimen, immerse the test panel vertically in the urine 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.
    4. Replace the cap and place the test panel on a non-absorbent flat surface.
    5. Start the timer and wait for the colored line(s) to appear.
    6. The result should be read at 5 minutes. Do not interpret the result after 10 minutes.CE Certified Carfentanyl Rapid Test Panel , rapid diagnostic test kits

 

 

INTERPRETATION OF RESULTS

 

(Please refer to the illustration above)

NEGATIVE:* Two lines appear. One colored line should be in the control line region (C), and another apparent colored line should be in the test line region (T). A negative result indicates that the Carfentanyl concentration is below the detectable level (500 ng/ml).

*NOTE: The shade of color in the test line region (T) may vary, but it should be considered negative whenever there is even a faint colored line.

POSITIVE: One colored line appears in the control line region (C). No line appears in the test line region (T). A positive result indicates that the Carfentanyl concentration exceeds the detectable level (500 ng/ml).

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. If the problem persists, discontinue using the lot immediately and contact your local distributor.

 

 

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.

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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