Multi-drug Rapid Test Device (Urine)

The Multi-drug Rapid Test Device (Urine) is rapid chromatographic immunoassays for the qualitative and simultaneous detection up to 22 of the following drugs in a variety of combinations in human urine. The designed cutoff concentrations for these drugs are as follows

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Product Overview

Test	Cut-off (ng/mL)
AMP(Amphetamine)	1000
THC(Marijuana)	50
COC (Cocaine)	300
PCP(Phencyclidine)	25
OPI(Opiate)	2000
MET(Methamphetamine )	1000
MTD(Methadone)	300
BAR(Secobarbital)	300
BZO(Oxazepam)	300
TCA(Nortriptyline)	1000
MDMA(Ecstasy)	500
BUP(Buprenorphine)	10
EDDP(Methadone metabolite)	100
PPX (Propoxyphene)	300
ETG(Ethylglucoronide)	500
K2(Synthetic cannabis)	50
TML(Tramadol)	100
MQL(Methaqualone)	300
COT(Cotinine)	200
FYL(Fentanyl)	200
OXY (Oxycodone)	100
KET (Ketamine)	1000

Test Procedure

Bring tests, specimens to room temperature (15-30°C) before use.

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Remove the test from its sealed pouch, and place it on a clean, level surface. For best results, the assay should be performed within one hour.

Place the device on a clean and level surface.

Using the provided dropper, and dispense 3 drops (approximately 120μl) into each sample well.

Avoid trapping air bubbles in the specimen well (S), and do not add any solution to the result area.

As the test begins to work, color will migrate across the membrane.

Wait for the colored band(s) to appear. The result should be read at 5 minutes. Do not interpret the result after 8 minutes.

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POSITIVE:

Only one colored band appears in the control region (C).No apparent 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.

NOTE:

The intensity of color in the test region (T) may vary depending on the concentration of analytes present in the specimen. Therefore, any shade of color in the test region should be considered negative. Note that this is a qualitative test only, and cannot determine the concentration of analytes in the specimen.

Insufficient specimen volume, incorrect operating procedure or expired tests are the most likely reasons for control band failure.