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                   Hangzhou AllTest Biotech CO.,LTD 

                                                      Your Reliable Rapid Test Partner!

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China good quality Custom Monoclonal Antibody on sale China good quality Hybridoma Monoclonal Antibody on sale
I like the products and service provided by AllTest. They really take our interest into consideration.

—— Mr John Smith England

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.

—— Ms Sheila

Whenever I have the requests,AllTest always give me the satisfied reply at the first time.

—— Mrs Julie Tschetter Belgium

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Multi-Drug Rapid Test Cup with Adulteration

Product Details:

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

Payment & Shipping Terms:

Minimum Order Quantity:500
Supply Ability:100 Million a year
Detailed Product Description

 

A rapid test for the simultaneous, qualitative detection of multiple drugs and drug metabolites CE certified

 

 

Applications: 

 

The Multi-Drug Rapid Test Cup is a rapid chromatographic immunoassay for the qualitative detection of multiple drugs and drug metabolites in urine at the following cut-off concentrations: 

Configurations of the Multi-Drug Rapid Test Cup come with any combination of the above listed drug analytes with or without S.V.T. 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 indicated.

 

 

Description: 

 

The Multi-Drug Rapid Test Cup is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes monoclonal antibodies to selectively detect elevated levels of specific drugs in urine.    

 

 

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 cup from the sealed pouch and use it within one hour.
  2. Donor provides specimen.
  3. Technician replaces and secures cap while the cup is on a flat surface.
  4. Technician dates and initials the security seal and attaches the security seal over the cup cap.
  5. Technician peels off label to reveal adulteration strip(s), if applicable.
  6. Technician peels off the label on the multi-drug test card to view results.
  7. Read the adulteration strips between 3-5 minutes (when applicable) compare the colors on the adulteration pads to the enclosed color chart. If the specimen indicates adulteration, refer to your Drug Free Policy for guidelines on adulterated specimens. We recommend not to interpret the drug test results and either retest the urine or collect another specimen.
  8. The drog strip result should be read at 5 minutes. Do not interpret the result after 10 minutes.

Multi-Drug Rapid Test Cup with Adulteration

 

INTERPRETATION OF RESULTS

 (Please refer to the illustration above)

 

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 urine 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.

 

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 urine 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 line appearing in the control 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 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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