(AMP) Drug of Abuse Rapid Test Kit
Product name
AMP Drug Test Rapid Test Kit
Sample type : URINE
Total 22 drug test items for choice:
AMP / BAR / BUP/ BZO/ COC /COT/ ETG / FYL / K2/ KET/ MAM /MDMA/ MET / MOP / MTD/ OPI / OXY/ PCP/ PPX / TCA/ THC/ TRA
Storage temperature
2°C - 30°C
Ingredients and Content
AMP Drug Rapid Test Kit (25 bags/ box)
Dropper (1 pc/bag)
Desiccant (1 pc/bag)
Urine cup(40 pcs/box)
[Intended use]
AMP Rapid Test is an immuno-chromatographic assay for the qualitative determination of the presence of Amphetamine . 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 Amphetamine the abuse test result, particularly when preliminary positive results are indicated.
Read the IFU completely before testing, allow the test device and specimens to equilibrate to room temperature (15～25℃) prior to testing
Method :
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.
[Result judgment]
* Positive (+): The wine red bands of control line C and detection line T indicated that the sample contained foot-and- mouth disease type A antibody.
* Negative (-): No color developed on the test T-ray, indicating that the sample did not contain foot-and-mouth disease type A antibody.
* Invalid: No QC Line C or Whiteboard present indicating incorrect procedure or invalid card. Please retest.
[Precautions]
1. Please use the test card within the guarantee period and within one hour after opening:
2. When testing to avoid direct sunlight and electric fan blowing;
3. Try not to touch the white film surface in the center of the detection card;
4. Sample dropper cannot be mixed, so as to avoid cross contamination;
5. Do not use sample diluent that is not supplied with this reagent;
6. After the use of detection card should be regarded as microbial dangerous goods processing;
[Application limitations]
This product is an immunological diagnostic kit and is only used to provide qualitative test results for clinical detection of pet diseases. If there is any doubt about the test results, please use other diagnostic methods (such as PCR, pathogen isolation test, etc.) to make further analysis and diagnosis of the detected samples. Consult your local veterinarian for pathological analysis.
[Storage and expiration]
This product should be stored at 2℃–40℃ in a cool, dry place away from light and not frozen; Valid for 24 months.
See the outer package for the expiration date and batch number.
