Description

Surgicare-Drug-Test-Kit-Pack

For professional in vitro diagnostic use only.

INTENDED USE:
The Blue Screen Dual-Drug One Step Methamphetamine/Marijuana Screening Test Panel (Urine) is a lateral flow chromatographic immunoassay for the qualitative detection of Methamphetamine and 11-nor-∆9-Tetrahydrocannabinol-9-carboxylic acid (∆9-THC-COOH) in human urine.

The Blue Screen Dual-Drug One Step Methamphetamine/Marijuana Screening Test Panel (Urine) yields positive results for the various drugs at the respective concentrations used: Methamphetamine 1000 ng/mL and THC 50 ng/mL. This is the suggested screening cut-off for positive specimens set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA)

DIRECTIONS:
Allow the test, urine specimen, and/or controls to reach room temperature (15o – 30oC) prior to testing.

Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.

Place the test device on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approximately 100 µl) to the specimen well (S) of the test device, and then start the timer. Avoid trapping air bubbles in the specimen well (S).

Wait for the colored line(s) to appear. Read the results at 5 minutes. It is important that the background is clear before the result is read. Do not interpret the result after 10 minutes.

INTERPRETATION OF RESULT:

POSITIVE:

MET Positive: No line appears in the MET test region (M) of the specific drug test. This positive result indicates that the Methamphetamine concentration exceeds the detectable cut-off level (1000 ng/mL)

THC Positive: No line appears in the THC test region (T) of the specific drug test. This positive result indicates that the Marijuana concentration exceeds the detectable cut-off level.

NEGATIVE: 3 lines appear. One red line should be in the control region (C) of the drug test, and two red or pink line should be in the test region (M/T) of the drug test.

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test using a new test panel. If the problem persists, discontinue using the lot immediately and contact your local distributor.