Product Overview
The Multi-drug Rapid Test Cup (Urine) is rapid chromatographic immunoassays for the qualitative and simultaneous detection up to twenty-eight of the following drugs in a variety of combinations in human urine.
TEST PROCEDURE
Bring tests, specimens to room temperature (15-30°C) before use.
Remove the cup from its sealed pouch and use it as soon as possible.
Provide a urine specimen in the cup and screw the cap on to the cup. Start the timer.
Date and initial the security seal label. Check the cap for tightness and attach the security seal label over the cap.
Remove the peel-off label.
Check the temperature strip label at 2-4 minutes after specimen collection. A green color will appear to indicate the temperature of the urine specimen. The proper range for an unadulterated specimen is 90-100°F (32 -38°C).
The result should be read at 5 minutes. Do not interpret the result after 8 minutes.
Positive test results must be confirmed by another test method. Send the cup and urine specimen with the security seal label intact to a toxicology laboratory for confirmation.
|
Pruduct |
Storage |
Specimen |
CE/FDA |
Model |
|
Multiple Drug Test Cup |
15-30℃ |
Urine |
CE, FDA |
005 |
In Vitro Diagnostic Reagents Products
Drugs combination available from 2 to 20 drugs
Instructions for use for testing of any combination of the following drugs
Amphetamine(AMP),Barbiturates(BAR), Benzoduazepines(BZO), Buprenorphine(BUP), Cocaine(COC),Cotinine(COT), Methadone metabolite (EDDP),Fentanyl (FYL), SyntheticCannabis(K2),Ketamine(KET), Methadone(MTD), Methamphetamine(MET),Methylenedioxymethamphetamine(MDMA),Morphine(MOP), Methaqualone (MQL), Opiate (OPI), Oxycodone (OXY), Phencyclidine (PCP),Propoxyphene (PPX), Marijuana(THC), Tricyclic Antidepressants (TCA),Tramadol (TML),D-Lysergic aciddiethylamide(LSD) Test,Ethyl Glucuronide(ETG) Test
Precautions
For in vitro diagnostic use only.
Do not use after the expiration date indicated on the package. Do not use the test if the foil pouch is damaged. Do not reuse tests.
All specimens should be considered potentially hazardous and handle in the same way as an infectious material.
Avoid cross-contamination of specimens by using a new specimen collection container and specimen pipette for each specimen obtained.
Read the entire procedure carefully prior to performing any tests.
The used testing materials should be discarded in accordance with local, state and/or federal regulations.
Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State.
FAQ
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