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Methamphetamine Rapid Test Cassette MET Rapid Test Kit For Urine Sample

Basic Information
Place of Origin: China
Brand Name: Dewei
Certification: ISO, CE, FDA
Model Number: MET-DU02
Minimum Order Quantity: 5000 units
Price: Negotiable
Packaging Details: 25test/box
Delivery Time: in 20 days
Payment Terms: L/C, T/T, Western Union
Supply Ability: 500,000pcs/day
Detail Information
Sample: Urine Certificate: ISO, CE, FDA
Type: Cassette Origin: China
Usage: Professional Use Shelf Life: 24 Months
High Light:

Methamphetamine Rapid Test Cassette

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MET Rapid Test Cassette

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FDA MET Rapid Test Kit


Product Description

Methamphetamine (MET) Rapid Test Cassette Drug of Abuse Rapid Test Kit for Urine Sample

 

Methamphetamine (MET) Rapid Test is a rapid, screening test for the qualitative detection of Methamphetamine and metabolites in human urine at specified cut off levels.

For professional use only.

For in vitro diagnostic use only.

 

【INTENDED USE】

Methamphetamine (MET) Rapid Test is an immuno-chromatographic assay for the qualitative determination of the presence of Methamphetamine (MET) listed in the table below.

Drug(Identifier)

Calibrator

Cut-off level

Methamphetamine (MET)

d-Methamphetamine

1000ng/mL

 

This assay provides only a preliminary analytical test result. Gas Chromatography/Mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to Methamphetamine (MET) of abuse test result, particularly when preliminary positive results are indicated.

 

【SUMMARY】

Methamphetamine is a potent sympathomimetic agent with therapeutic applications. Acute higher doses lead to enhanced stimulation of the central nervous system and induce euphoria, alertness, and a sense of increased energy and power. More acute responses produce anxiety, paranoia, psychotic behavior, and cardiac dysrhythmias. The pattern of psychosis which may appear at half-life of about 15 hours is excreted in urine as amphetamine and oxidized as deaminated and hydroxylated derivatives. However, 40% of methamphetamine is excreted unchanged. Thus the presence of the parent compound in the urine indicates methamphetamine use.

 

【PRINCIPLE】

Methamphetamine (MET) Rapid Test is a competitive immunoassay that is used to screen for the presence of Methamphetamine (MET) and metabolites in urine. It is chromatographic absorbent device in which, drugs within a urine sample, competitively combined to a limited number of drug monoclonal antibody (mouse) conjugate binding sites.

 

When the test is activated, the urine is absorbed into test by capillary action, mixes with the respective drug monoclonal antibody conjugate, and flows across a pre-coated membrane. When drug within the urine sample is below the detection level of the test, respective drug monoclonal antibody conjugate binds to the respective drug-protein conjugate immobilized in the Test Region (T) of the test . This produces a colored Test line in the Test Region (T) of the , which, regardless of its intensity, indicates a negative test result.

 

When sample drug levels are at or above the detection level of the test, the free drug in the sample binds to the respective drug monoclonal antibody conjugate, preventing the respective drug monoclonal antibody conjugate from binding to the respective drug-protein conjugate immobilized in the Test Region (T) of the device. This prevents the development of a distinct colored band in the test region, indicating a preliminary positive result.

 

To serve as a procedure control, a colored line will appear at the Control Region (C) of , if the test has been performed properly.

 

【WARNINGS AND PRECAUTIONS】

  • Immunoassay for in vitro diagnostic use only.
  • Do not use after expiration date.
  • The test should remain in the sealed pouch until use.
  • The used test should be discarded according to local regulations.

 

【CONTENTS】

  • Drug Test.
  • Desiccant.
  • Leaflet with instruction for use.

STORAGE AND STABILITY

  • The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
  • The test must remain in the sealed pouch until use.
  • Keep away from direct sunlight, moisture and heat.
  • Do not freeze.
  • Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.

OPERATION

Test must be in room temperature (15ºC to 30ºC)

  1. Donor collects urine specimen in a urine cup.
  2. Open the sealed pouch by tearing along the notch. Remove the test from the pouch and place it on a level surface.
  3. Hold the sample dropper vertically, and add exactly three drops of the urine specimen into the sample well.
  4. The result should be read at 5 minutes. Do not interpret the result after 10 minutes. See the illustration below.

【INTERPRETATION OF RESULTS】

Preliminary positive (+)

Only one colored band appears, in the control region (C). No colored band appears in the test region (T).

Negative (-)

Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).

Invalid

Control band fails to appear. Results from any test which has not produced a control band at the specified read time must be discarded. Please review the procedure and repeat with a new test. If the problem persists, discontinue using the kit immediately and contact your local distributor.

 

 

 

Contact Details
Bonnie He

Phone Number : +8613030247038

WhatsApp : +008615267039708