Oxycodone OXY Rapid Test Cassette DOA Rapid Test Kit For Urine Sample CE

FDA CE Oxycodone (OXY) Rapid Test Cassette DOA Rapid Test Kit for Urine Sample

Oxycodone (OXY) Rapid Test is a rapid, screening test for the qualitative detection of Oxycodone and metabolites in human urine at specified cut oflevels.

For professional use only.

For in vitro diagnostic use only.

【INTENDED USE】

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

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 Oxycodone (OXY) of abuse test result, particularly when preliminary positive results are indicated.

【SUMMARY】

Oxycodone is an analgesic, which works by depressing the central nervous system. Oxycodone is abused for its opiate-like effects. In addition to its equal potency to morphine in analgesic effects, it is also equipotent to morphine in relieving abstinence symptoms from chronic opiate (heroin, morphine) use. For this reason, it is often used to alleviate or prevent the onset of opiate withdrawal by street users of heroin and methadone. The drug is most often administered orally. Like other opiates, Oxycodone can also depress the respiratory system resulting in suffocation and death when overdosed. Oxycodone is very addictive, both physically and psychologically. Some physical indications of Oxycodone abuse include extreme loss of appetite and weight, cramps, nausea, vomiting, excessive scratching and complaint of itching, excessive sweating, constipation, pin-point pupils and watery eyes, reduced vision, drowsiness, euphoria, trance-like states, excessive thirst, tremors, twitching, irritability, hallucinations and lethargy.

【PRINCIPLE】

Oxycodone (OXY) Rapid Test is a competitive immunoassay that is used to screen for the presence of Oxycodone (OXY) 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 Test, 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 Test, 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.

                                   Cassette/Device