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Powder Drug Abuse Test Kit Accurate Opiate One Step Panel 2000 Ng / Ml

Basic Information
Place of Origin: China
Brand Name: AllTest
Certification: CE, ISO13485
Model Number: DOP-X14
Minimum Order Quantity: N/A
Price: Negotiation
Packaging Details: 25 cassette/box
Delivery Time: 2-4 Weeks
Payment Terms: Ex works
Supply Ability: 10 M tests/month
Format: Panel Specimen: Powder
Kit Size: 25T/Kit Storage: 2-30℃
Cut-off: 2000 Ng/ml Certificate: CE
High Light:

rapid diagnostic test kits

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home drug test kits

 

Accurate Opiate One Step Panel 2000 ng/ml Powder Drug Abuse Test Kit Wiht CE

 

 

Applications and Description:

 

Opiate refers to any drug that is derived from the opium poppy, including the natural products, Morphine and Codeine, and the semi-synthetic drugs such as heroin. Opioid is more general, referring to any drug that acts on the opioid receptor.
Opioid analgesics comprise a large group of substance which control pain by depressing the central nervous system. Large doses of Morphine can produce higher tolerance levels and physiological dependency in users, and may lead to substance abuse. Morphine is excreted unmetabolized, and is also the major metabolic product of codeine and heroin. Morphine is detectable in the urine for several days after an opiate dose.
The OPI Rapid Test Cassette (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 Morphine in urine. The OPI Rapid Test Cassette (Urine) yields a positive result when Morphine in urine exceeds 2,000 ng/mL. This is the suggested screening cut-off for positive specimens set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA).

 

How to 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
 
1. Wipe with the panel over the surface in which the drugs are expected
2. Take off the cap of supplied tube;
3. Fill all buffers from the supplied tube of buffer into the protection cover.
4. Insert the Multi Test slowly and carefully into the protection cover with buffer.
5. Wait for lines to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.

Powder Drug Abuse Test Kit Accurate Opiate One Step Panel 2000 Ng / Ml 0

 
FOR SOLIDS
1. Open the tube and put the solid in to the buffer.
2. Close the tube with dropper and cap. Shake it a short time. Wait for 30 sec.
3. Take off the cap of supplied tube;
4. Fill all buffers with dissolved substances into the protection cover.
5. Insert the Multi Test slowly and carefully into the protection cover with buffer.
6. Wait for lines to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.

Powder Drug Abuse Test Kit Accurate Opiate One Step Panel 2000 Ng / Ml 1


 

INTERPRETATION OF RESULTS
(Please refer to the illustration above)
Powder Drug Abuse Test Kit Accurate Opiate One Step Panel 2000 Ng / Ml 2

NEGATIVE:* A colored line appears in the Control region (C) and colored 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 colored lines(s) in the Test region (T) may vary. The result should be considered negative whenever there is even a faint line.

Powder Drug Abuse Test Kit Accurate Opiate One Step Panel 2000 Ng / Ml 3

POSITIVE: A colored 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.


Powder Drug Abuse Test Kit Accurate Opiate One Step Panel 2000 Ng / Ml 4

 

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.

Contact Details
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Phone Number : +8615857153722

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